Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols as phosphodiesterase inhibitors

ABSTRACT

Derivatives of 1-phenyl-2-pyridinyl alkyl alcohols are useful as inhibitors of the phosphodiesterase 4 (PDE4) enzyme and the treatment of certain conditions such as COPD.

CROSS REFERENCES TO RELATED APPLICATIONS

This application claims priority to European Patent Application No. 11168853.7, filed on Jun. 6, 2011, which is incorporated herein by reference in its entirety.

BACKGROUND OF THE INVENTION

1. Field of the Invention

The present invention relates to inhibitors of the phosphodiesterase 4 (PDE4) enzyme. More particularly, the present invention relates to compounds that are derivatives of 1-phenyl-2-pyridinyl alkyl alcohols, methods of preparing such compounds, compositions containing them, and therapeutic uses of such compounds and compositions.

2. Discussion of the Background

Airway obstruction characterizes a number of severe respiratory diseases including asthma and chronic obstructive pulmonary disease (COPD). Events leading to airway obstruction include edema of airway walls, increased mucous production and inflammation.

Drugs for treating respiratory diseases such as asthma and COPD are currently administered through inhalation. One of the advantages of the inhalatory route over the systemic one is the possibility of delivering the drug directly at site of action, reducing systemic side-effects, thus resulting in a more rapid clinical response and a higher therapeutic ratio.

Inhaled corticosteroids are the current maintenance therapy of choice for asthma and together with bronchodilator beta₂-agonists for acute symptom relief, they form the mainstay of current therapy for the disease. The current management of COPD is largely symptomatic by means of bronchodilating therapy with inhaled anticholinergics and inhaled beta₂-adrenoceptor agonists. However, corticosteroids do not reduce the inflammatory response in COPD as they do in asthma.

Another class of therapeutic agents which has been widely investigated in view of its anti-inflammatory effects for the treatment of inflammatory respiratory diseases such as asthma and COPD is represented by the inhibitors of the enzymes phosphodiesterases (PDEs), in particular of the phosphodiesterase type 4 (hereinafter referred to as PDE4).

Various compounds acting as PDE4 inhibitors have been disclosed in the prior art. However, the usefulness of several PDE4 inhibitors of the first-generation such as rolipram and piclamilast has been limited due to their undesirable side effects. Said effects include nausea and emesis due to their action on PDE4 in the central nervous system and gastric acid secretion due to the action on PDE4 in parietal cells in the gut.

The cause of said side effects has been widely investigated. It has been found that PDE4 exists in two distinct forms representing different conformations, that were designated as high affinity rolipram binding site or HPDE4, especially present in the central nervous system and in parietal cells, and low affinity rolipram binding site or LPDE4 (see Jacobitz, S et al., Mol. Pharmacol., 1996, 50, 891-899, which is incorporated herein by reference in its entirety), which is found in the immune and inflammatory cells. While both forms appear to exhibit catalytic activity, they differ with respect to their sensitivity to inhibitors. In particular compounds with higher affinity for LPDE4 appear less prone to induce side-effects such as nausea, emesis and increased gastric secretion.

The effort of targeting LPDE4 has resulted in a slight improvement in the selectivity for the second-generation PDE4 inhibitors such as roflumilast. Nonetheless, roflumilast is under dosed in order to achieve an acceptable side effect profile.

Other classes of compounds acting as PDE4 inhibitors have also been disclosed. For example, EP 1 634 606 discloses, among others, ketone derivatives like benzofuran or 1,3-benzodioxole derivatives.

WO 94/02465 discloses, among others, ketone derivatives of general formula

wherein R₁ is lower alkyl and R₂ may be alkyl, alkenyl, cycloalkyl, cycloalkyl, cycloalkenyl, cyclothioalkyl or cyclothioalkenyl.

WO 95/35281 in the name of Celltech Therapeutics relates to tri-substituted phenyl derivatives.

WO 2009/018909 discloses derivatives of 1-phenyl-2-pyridinyl alkyl alcohols which have general formula below reported

as inhibitors of phosphodiesterase 4 (PDE4) enzyme.

WO 2009/077068 discloses further derivatives of 1-phenyl-2-pyridinyl alkyl alcohols which have general formula below reported

as inhibitors of phosphodiesterase 4 (PDE4) enzyme.

WO 2010/089107 discloses further derivatives of 1-phenyl-2-pyridinyl alkyl alcohols which have general formula below reported

as inhibitors of phosphodiesterase 4 (PDE4) enzyme.

Although several PDE4 inhibitors have been disclosed so far as above reported, there is still a need for further PDE4 inhibitors. Particularly, there is still a need for further PDE4 inhibitors endowed with a high affinity for PDE4 enzyme. Particularly advantageous would also be the identification of further PDE4 inhibitors endowed with a high affinity for PDE4 enzyme and which would show an appropriate developability profile as an inhalation treatment for example in terms of reduced side effects.

Such reduction of side effects may be achieved, by way of example, through a low systemic exposure of the drug; an appropriate profile in terms of some pharmacokinetic characteristics, especially metabolic clearance, may be thus key to this goal.

SUMMARY OF THE INVENTION

Accordingly, it is one object of the present invention to provide novel PDE4 inhibitors endowed with a high affinity for PDE4 enzyme.

It is another object of the present invention to provide novel PDE4 inhibitors endowed with a high affinity for PDE4 enzyme and which show an appropriate developability profile as an inhalation treatment for example in terms of reduced side effects.

It is another object of the present invention to provide novel pharmaceutical compositions which contain such PDE4 inhibitor.

It is another object of the present invention to provide novel combinations of such a PDE4 inhibitor and one or more other active agents.

It is another object of the present invention to provide novel methods of treating a condition such as COPD by administering such a PDE4 inhibitor.

These and other objects, which will become apparent during the following detailed description, have been achieved by the inventors' discovery of certain new PDE4 inhibitors. Thus, the present invention addresses the above mentioned object by providing the compounds of the invention.

Thus, the present invention is directed to compounds acting as inhibitors of the phosphodiesterase 4 (PDE4) enzyme, methods of preparing said compounds, compositions containing them and therapeutic use thereof.

In particular, the present invention is directed to derivatives of 1-phenyl-2-pyridinyl alkyl alcohols of general formula (I):

wherein:

-   R₁ is selected from the group consisting of:     -   H;     -   (C₃-C₇)cycloalkylcarbonyl;     -   (C₁-C₆)alkyl, optionally substituted by one or more substituents         selected from (C₃-C₇)cycloalkyl or (C₅-C₇)cycloalkenyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)cycloalkyl;     -   (C₅-C₇)cycloalkenyl;     -   (C₂-C₆)alkenyl; and     -   (C₂-C₆)alkynyl; -   R₂ is selected from the group consisting of:     -   H;     -   (C₃-C₇)cycloalkylcarbonyl;     -   (C₁-C₆)alkyl, optionally substituted by one or more substituents         selected from (C₃-C₇)cycloalkyl or (C₅-C₇)cycloalkenyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)cycloalkyl;     -   (C₅-C₇)cycloalkenyl;     -   (C₂-C₆)alkenyl; and     -   (C₂-C₆)alkynyl;     -   or, when R₁₉ is different from hydrogen, R₂ forms together with         R₁₉ a group of formula (x) as below defined;     -   or R₁ and R₂, together with the interconnecting atoms, form a         2,2-difluoro-1,3-dioxolane ring of formula (q) fused to the         phenyl moiety which bears groups —OR₁ and —OR₂, wherein         asterisks indicate carbon atoms shared with such phenyl ring:

R₁₉ is hydrogen or, if different from hydrogen, it forms together with R₂ a group of formula (x) wherein bonds labeled with (1) and (2) indicate the points of attachment for group (x) to atoms bearing groups R₁₉ and R₂ respectively

in such a way that R₂ and R₁₉ together with the interconnecting atoms form a ring of formula (w) which is fused to phenyl ring which bears groups —OR₂ and R₁₉, wherein asterisks indicate carbon atoms shared with such phenyl ring:

R₃ is one or more substituents independently selected from the group consisting of H, CN, NO₂, CF₃ and a halogen atom; Z is a group —(CH₂)_(n)— wherein n is 0 or 1; A is a saturated and monocyclic (C₃-C₇)heterocycloalkylene group; K is selected from the group consisting of:

-   -   —(CH₂)_(m)C(O)R₄ wherein m may be 0 or 1;     -   —C(O)(CH₂)_(j)R₄, wherein j may be 1 or 2;     -   —SO₂(CH₂)_(p)R₄ wherein p may be zero, 1 or 2;     -   —(CH₂)_(y)SO₂R₄ wherein y may be 1 or 2;     -   —(CH₂)_(z)R₄ wherein z may be 1 or 2; and     -   —C(O)(CH₂)₂SO₂R₄;     -   R₄ is a ring system, that is a mono- or bicyclic ring which may         be saturated, partially unsaturated or fully unsaturated, such         as aryl, (C₃-C₈)cycloalkyl, (C₃-C₇)heterocycloalkyl or         heteroaryl, such ring being optionally substituted by one or         more groups R₅ which may be the same or different, and which are         independently selected from the group consisting of:         -   (C₁-C₆)alkyl optionally substituted by one or more groups             independently selected in the list consisting of:             (C₃-C₇)cycloalkyl, —OH and a group —NR₁₈C(O)(C₁-C₄) alkyl,             wherein R₁₈ is hydrogen or (C₁-C₄)alkyl;         -   (C₃-C₇)heterocycloalkyl;         -   5 or 6-membered heteroaryl which is optionally substituted             by one or two groups (C₁-C₄)alkyl;         -   (C₁-C₆)haloalkyl;         -   (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;         -   a group —OR₆ wherein R₆ is selected from the group             consisting of             -   H:             -   (C₁-C₆)haloalkyl;             -   a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl;             -   a group —C(O)R_(D) wherein R₇ is (C₁-C₄)alkyl;             -   —(C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇) cycloalkyl or by a group —NR₈R₉ as below                 defined; and             -   (C₃-C₇)cycloalkyl;         -   a group —SR₂₀ wherein R₂₀ is selected from the group             consisting of             -   —H:             -   (C₁-C₆)haloalkyl;             -   a group —C(O)R₇ wherein R₇ is (C₁-C₄)alkyl;             -   (C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇) cycloalkyl or by a group —NR₈R₉; and             -   (C₃-C₇)cycloalkyl;         -   halogen atoms;         -   CN;         -   NO₂;         -   NR₈R₉ wherein R₈ and R₉ are different or the same and are             independently selected from the group consisting of:             -   H;             -   (C₁-C₄)alkylene-NR₁₃R₁₄ wherein R₁₃ and R₁₄ are                 different or the same and are independently selected                 from the group consisting of: H and (C₁-C₆)alkyl, which                 is optionally substituted with (C₃-C₇)cycloalkyl or                 (C₃-C₇) heterocycloalkyl; or they form with the nitrogen                 atom to which they are linked a saturated or partially                 saturated (C₃-C₇)heterocyclic ring;             -   (C₁-C₆)alkyl, optionally substituted with                 (C₃-C₇)cycloalkyl, (C₃-C₇)heterocycloalkyl, a group —OH                 or (C₁-C₆)alkoxyl;             -   a group —SO₂R₁₅, wherein R₁₅ is selected in the group                 consisting of: (C₁-C₄)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; and phenyl optionally                 substituted by one or more (C₁-C₆)alkyl, halogen or a                 group —OH;             -   a group —C(O)R₁₆, wherein R₁₆ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   a group —C(O)OR₁₇, wherein R₁₇ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   or they form with the nitrogen atom to which they are                 linked a saturated or partially saturated heterocyclic                 ring, which is optionally substituted by one or more                 (C₁-C₆)alkyl or oxo groups;         -   (C₁-C₄)alkylene-NR₈R₉ as above defined;         -   COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl;         -   oxo;         -   —SO₂R₁₁ wherein R₁₁ is (C₁-C₄)alkyl, OH or NR₈R₉ wherein R₈             and R₉ are as defined above;         -   —COOR₁₂ wherein R₁₂ is H, (C₁-C₄)alkyl or             (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined             above; and         -   —CONR₈R₉ wherein R₈ and R₉ are as defined above;     -   wherein groups R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅,         R₁₆, R₁₇, R₁₈, R₁₉ and R₂₀ may assume the same or different         meanings at each occurrence, if present in more than one group;         their N-oxides on the pyridine ring, and pharmaceutically         acceptable salts, or solvates thereof.

In a preferred embodiment, the invention is directed to derivatives of 1-phenyl-2-pyridinyl alkyl alcohols of general formula (IG):

wherein: R₁ is selected from the group consisting of:

-   -   H;     -   (C₃-C₇)cycloalkylcarbonyl;     -   (C₁-C₆)alkyl, optionally substituted by one or more substituents         selected from (C₃-C₇)cycloalkyl or (C₅-C₇)cycloalkenyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)cycloalkyl;     -   (C₅-C₇)cycloalkenyl;     -   (C₂-C₆)alkenyl; and     -   (C₂-C₆)alkynyl;         R₂ is selected from the group consisting of:     -   H;     -   (C₃-C₇)cycloalkylcarbonyl;     -   (C₁-C₆)alkyl, optionally substituted by one or more substituents         selected from (C₃-C₇)cycloalkyl or (C₅-C₇)cycloalkenyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)cycloalkyl;     -   (C₅-C₇)cycloalkenyl;     -   (C₂-C₆)alkenyl; and     -   (C₂-C₆)alkynyl;     -   or R₁ and R₂, together with the interconnecting atoms, form a         2,2-difluoro-1,3-dioxolane ring of formula (q) fused to the         phenyl moiety which bears groups —OR₁ and —OR₂, wherein         asterisks indicate carbon atoms shared with such phenyl ring:

R₁₉ is hydrogen; R₃ is one or more substituents independently selected from the group consisting of H, CN, NO₂, CF₃ and a halogen atom; Z is a group —(CH₂)_(n)— wherein n is 0 or 1; A is a saturated and monocyclic (C₃-C₇)heterocycloalkyl-ene group; K is selected from the group consisting of:

-   -   —(CH₂)_(m)C(O)R₄ wherein m may be 0 or 1;     -   —C(O)(CH₂)_(j)R₄, wherein j may be 1 or 2;     -   —SO₂ (CH₂)_(p)R₄ wherein p may be zero, 1 or 2;     -   —(CH₂)_(y)SO₂R₄ wherein y may be 1 or 2;     -   —(CH₂)_(n)R₄ wherein z may be 1 or 2; and     -   —C(O)(CH₂)₂SO₂R₄;     -   R₄ is a ring system, that is a mono- or bicyclic ring which may         be saturated, partially unsaturated or fully unsaturated, such         as aryl, (C₃-C₈)cycloalkyl, (C₃-C₇)heterocycloalkyl or         heteroaryl, such ring being optionally substituted by one or         more groups R₅ which may be the same or different, and which are         independently selected from the group consisting of:         -   (C₁-C₆)alkyl optionally substituted by one or more groups             independently selected in the list consisting of:             (C₃-C₇)cycloalkyl, —OH and a group —NR₁₈C(O)(C₁-C₄)alkyl,             wherein R₁₈ is hydrogen or (C₁-C₄)alkyl;         -   (C₃-C₇)heterocycloalkyl;         -   5 or 6-membered heteroaryl which is optionally substituted             by one or two groups         -   (C₁-C₄)alkyl;         -   (C₁-C₆)haloalkyl;         -   (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;         -   a group —OR₆ wherein R₆ is selected from the group             consisting of             -   —H:             -   —(C₁-C₆)haloalkyl;             -   a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl;             -   a group —C(O)R₇ wherein R₇ is (C₁-C₄)alkyl;             -   (C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇) cycloalkyl or by a group —NR₈R₉; and             -   (C₃-C₇)cycloalkyl;         -   a group —SR₂₀ wherein R₂₀ is selected from the group             consisting of             -   —H:             -   (C₁-C₆)haloalkyl;             -   a group —C(O)R_(D) wherein R₇ is (C₁-C₄)alkyl;             -   (C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇) cycloalkyl or by a group —NR₈R₉ as below                 defined; and             -   (C₃-C₇)cycloalkyl;         -   halogen atoms;         -   CN;         -   NO₂;         -   NR₈R₉ wherein R₈ and R₉ are different or the same and are             independently selected from the group consisting of:             -   H;             -   —(C₁-C₄)alkylene-NR₁₃R₁₄ wherein R₁₃ and R₁₄ are                 different or the same and are independently selected                 from the group consisting of: H and (C₁-C₆)alkyl, which                 is optionally substituted with (C₃-C₇)cycloalkyl or                 (C₃-C₇)heterocycloalkyl; or they form with the nitrogen                 atom to which they are linked a saturated or partially                 saturated (C₃-C₇)heterocyclic ring;             -   (C₁-C₆)alkyl, optionally substituted with                 (C₃-C₇)cycloalkyl, (C₃-C₇)heterocycloalkyl, a group —OH                 or (C₁-C₆)alkoxyl;             -   a group —SO₂R₁₅, wherein R₁₅ is selected in the group                 consisting of: (C₁-C₄)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; and phenyl optionally                 substituted by one or more (C₁-C₆)alkyl, halogen or a                 group —OH;             -   a group —C(O)R₁₆, wherein R₁₆ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   a group —C(O)OR₁₇, wherein R₁₇ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   or they form with the nitrogen atom to which they are                 linked a saturated or partially saturated heterocyclic                 ring, which is optionally substituted by one or more                 (C₁-C₆)alkyl or oxo groups;         -   (C₁-C₄)alkylene-NR₈R₉ as above defined;         -   COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl;         -   oxo;         -   —SO₂R₁₁ wherein R₁₁ is (C₁-C₄)alkyl, OH or NR₈R₉ wherein R₈             and R₉ are as defined above;         -   —COOR₁₂ wherein R₁₂ is H or (C₁-C₄)alkyl or             (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined             above; and         -   —CONR₈R₉ wherein R₈ and R₉ are as defined above;     -   wherein groups R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅,         R₁₆, R₁₇, R₁₈, R₁₉ and R₂₀ may assume the same or different         meanings at each occurrence, if present in more than one group;         their N-oxides on the pyridine ring, and pharmaceutically         acceptable salts, or solvates thereof.

In another preferred embodiment, invention is directed to derivatives of 1-phenyl-2-pyridinyl alkyl alcohols of general formula (IL):

wherein: R₁ and R₂ are different or the same and are independently selected from the group consisting of:

-   -   H;     -   (C₃-C₇)cycloalkylcarbonyl;     -   (C₁-C₆)alkyl, optionally substituted by one or more substituents         selected from (C₃-C₇)cycloalkyl or (C₅-C₇)cycloalkenyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)cycloalkyl;     -   (C₅-C₇)cycloalkenyl;     -   (C₂-C₆)alkenyl; and     -   (C₂-C₆)alkynyl;         R₃ is one or more substituents independently selected from the         group consisting of H, CN,         NO₂, CF₃ and a halogen atom;         Z is a group —(CH₂)_(n)— wherein n is 0 or 1;         A is a saturated and monocyclic (C₃-C₇)heterocycloalkyl-ene         group;         K is selected from the group consisting of:     -   —(CH₂)_(m)C(O)R₄ wherein m may be 0 or 1;         -   —C(O)(CH₂)R₄;         -   —SO₂ (CH₂)_(p)R₄ wherein p may be zero or 1;         -   —CH₂SO₂R₄; and         -   —CH₂R₄;     -   R₄ is a ring system, that is a mono- or bicyclic ring which may         be saturated, partially unsaturated or fully unsaturated, such         as aryl, (C₃-C₈)cycloalkyl, (C₃-C₇)heterocycloalkyl or         heteroaryl, such ring being optionally substituted by one or         more groups R₅ which may be the same or different, and which are         independently selected from the group consisting of:         -   (C₁-C₆)alkyl optionally substituted by one or more             (C₃-C₇)cycloalkyl;         -   (C₃-C₇)heterocycloalkyl;         -   (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;         -   a group —OR₆ wherein R₆ is selected from the group             consisting of             -   —H:             -   (C₁-C₆)haloalkyl;             -   a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl;             -   a group —C(O)R₇ wherein R₇ is (C₁-C₄)alkyl;             -   (C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇) cycloalkyl or by a group —NR₈R₉; and             -   (C₃-C₇)cycloalkyl;         -   a group —SR₂₀ wherein R₂₀ is selected from the group             consisting of             -   —H:             -   —(C₁-C₆)haloalkyl;             -   a group —C(O)R_(D) wherein R₇ is (C₁-C₄)alkyl;             -   (C₁-C₁₀)alkyl optionally substituted by one or more                 (C₃-C₇)cycloalkyl or by a group —NR₈R₉ as below defined;                 and             -   (C₃-C₇)cycloalkyl;         -   halogen atoms;         -   CN;         -   NO₂;         -   NR₈R₉ wherein R₈ and R₉ are different or the same and are             independently selected from the group consisting of:             -   H;             -   (C₁-C₄)alkylene-NR₁₃R₁₄ wherein R₁₃ and R₁₄ are                 different or the same and are independently selected                 from the group consisting of: H and (C₁-C₆)alkyl, which                 is optionally substituted with (C₃-C₇)cycloalkyl or                 (C₃-C₇)heterocycloalkyl; or they form with the nitrogen                 atom to which they are linked a saturated or partially                 saturated (C₃-C₇)heterocyclic ring;             -   (C₁-C₆)alkyl, optionally substituted with                 (C₃-C₇)cycloalkyl, (C₃-C₇)heterocycloalkyl, a group —OH                 or (C₁-C₆)alkoxyl;             -   a group —SO₂R₁₅, wherein R₁₅ is selected in the group                 consisting of: (C₁-C₄)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; and phenyl optionally                 substituted by one or more (C₁-C₆)alkyl, halogen or a                 group —OH;             -   a group —C(O)R₁₆, wherein R₁₆ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   a group —C(O)OR₁₇, wherein R₁₇ is selected in the group                 consisting of: (C₁-C₆)alkyl optionally substituted by                 (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl;                 (C₃-C₇)heterocycloalkyl; phenyl optionally substituted                 by one or more (C₁-C₆)alkyl, halogen or —OH; and a group                 —NH₂;             -   or they form with the nitrogen atom to which they are                 linked a saturated or partially saturated heterocyclic                 ring, which is optionally substituted by one or more                 (C₁-C₆)alkyl or oxo groups;         -   (C₁-C₄)alkylene-NR₈R₉ as above defined;         -   COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl;         -   oxo;         -   —SO₂R₁₁ wherein R₁₁ is (C₁-C₄)alkyl, OH or NR₈R₉ wherein R₈             and R₉ are as defined above;         -   —COOR₁₂ wherein R₁₂ is H or (C₁-C₄)alkyl or             (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined             above; and         -   —CONR₈R₉ wherein R₈ and R₉ are as defined above;     -   wherein groups R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅,         R₁₆, R₁₇ and R₂₀ may assume the same or different meanings at         each occurrence, if present in more than one group; their         N-oxides on the pyridine ring, and pharmaceutically acceptable         salts, or solvates thereof.

The present invention further provides the corresponding N-oxides on the pyridine ring of compounds of formula (I).

The present invention also provides the pharmaceutically acceptable salts and/or solvates thereof.

The term “pharmaceutically acceptable salts”, as used herein, refers to derivatives of compounds of formula (I) or of their corresponding N-oxides on the pyridine ring wherein the parent compound is suitably modified by converting any of the free acid or basic groups, if present, into the corresponding addition salt with any base or acid conventionally intended as being pharmaceutically acceptable.

Suitable examples of said salts may thus include mineral or organic acid addition salts of basic residues such as amino groups, as well as mineral or organic acid residues such as carboxylic groups.

Cations of inorganic bases which can be suitably used to prepare salts within the invention comprise ions of alkali or alkaline earth metals such as potassium, sodium, calcium or magnesium.

Those obtained by reacting the main compound, functioning as a base, with an inorganic or organic acid to form a salt comprise, for example, salts of hydrochloric acid, sulfuric acid, phosphoric acid, methane sulfonic acid, camphor sulfonic acid, oxalic acid, maleic acid, succinic acid and citric acid.

Those skilled in the art of organic chemistry will appreciate that many organic compounds can form complexes with solvents in which they are reacted or from which they are precipitated or crystallized. These complexes are known as “solvates”. Pharmaceutically acceptable solvates of compound of the invention are within the scope of the invention.

Included within the scope of the present invention are also polymoprhs and crystalline forms of compounds of formula (I), of their N-oxides on the pyridine ring, or of pharmaceutically acceptable salts, or solvates thereof.

Hereinafter, compounds of formula (I), (IG), (IL), corresponding N-Oxides on the pyridine ring, embodiments, enantiomers, diastereoisomers thereof, their pharmaceutically acceptable salts and solvates, and polymorphs or crystalline forms thereof defined in any aspect of the invention (except intermediate compounds described in the chemical processes) are referred to as “compounds of the invention”.

The present invention further provides a process for the preparation of compounds of the invention.

The present invention also provides pharmaceutical compositions of compounds of the invention either alone or in combination, in admixture with one or more pharmaceutically acceptable carriers.

In a further aspect the present invention provides the use of the compounds of the present invention as a medicament.

In another aspect the present invention provides the use of the compounds of the present invention for the manufacture of a medicament.

In particular, the present invention provides the use of the compounds of the present invention for the prevention and/or treatment of any disease characterized by phosphodiesterase 4 (PDE4) overactivity and/or wherein an inhibition of PDE4 activity is desirable.

In particular, the compounds of the present invention alone or combined with other active ingredients may be administered for the prevention and/or treatment of a disease the respiratory tract characterized by airway obstruction such as asthma and COPD.

In a further aspect, the present invention provides the use of compounds of the present invention for the preparation of a medicament for the prevention and/or treatment of any disease characterized by phosphodiesterase 4 (PDE4) overactivity and/or wherein an inhibition of PDE4 activity is desirable.

Moreover, the present invention provides methods for prevention and/or treatment of any disease wherein PDE4 inhibition is desiderable, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound of the present invention.

DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS

The term “halogen atoms” as used herein includes fluorine, chlorine, bromine, and iodine, preferably chlorine.

As used herein, the term “(C₁-C_(x))alkyl” where x is an integer greater than 1, refers to straight-chained and branched alkyl groups wherein the number of constituent carbon atoms is in the range 1 to x. Particular alkyl groups are methyl, ethyl, n-propyl, isopropyl, and t-butyl.

By analogy, the term “(C₁-C_(x))alkylene”, refers to a divalent (C₁-C_(x))alkyl radical, wherein (C₁-C_(x))alkyl is as above defined.

The term “(C_(I)-C_(x))alkoxyl” where x is an integer greater than 1, refers to straight-chained and branched alkoxy groups wherein the number of constituent carbon atoms is in the range 1 to x. Particular alkyl groups are methoxyl, ethoxyl, n-propoxyl, isopropoxyl, and t-butoxyl.

The expressions “(C₁-C_(x))haloalkyl” refer to the above defined “(C₁-C_(x))alkyl” groups wherein one or more hydrogen atoms are replaced by one or more halogen atoms, which can be the same or different from each other.

Examples of said (C₁-C₆)haloalkyl groups may thus include halogenated, poly-halogenated and fully halogenated alkyl groups wherein all of the hydrogen atoms are replaced by halogen atoms, e.g. trifluoromethyl or difluoro methyl groups.

The term “(C₃-C_(y))cycloalkyl”, where y is an integer greater than or equal to 3, refers to saturated cyclic hydrocarbon groups containing from 3 to y ring carbon atoms. Examples include cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, and cycloheptyl.

The derived expression “(C₃-C_(y))heterocycloalkyl” refers to monocyclic (C₃-C_(y))cycloalkyl groups, in which at least one ring carbon atom is replaced by a heteroatom (e.g. N, NH, S or O). Non-limiting examples of (C₃-C_(y))heterocycloalkyl are represented by: pyrrolidinyl, thiazolidinyl, piperazinyl, piperidnyl, morpholinyl, thiomorpholinyl, and azetidinyl.

By analogy, the term “(C₃-C_(y))heterocycloalkyl-ene”, refers to a divalent (C₃-C_(y))heterocycloalkyl radical, wherein (C₃-C_(y))heterocycloalkyl is as above defined.

The expression “(C₃-C_(y))cycloalkylcarbonyl” refers to (C₃-C_(y))cycloalkylCO— groups wherein the group “(C₃-C_(y))cycloalkyl” has the meaning above defined.

The term “(C₂-C₆)alkenyl” refers to straight or branched, conjugated or non-conjugated, carbon chains with one or more double bonds, in cis or trans configuration, wherein the number atoms is in the range 2 to 6.

The term “(C₅-C_(z))cycloalkenyl”, where z is an integer greater than or equal to 5, refers to cyclic hydrocarbon groups containing from 5 to z ring carbon atoms and one or more double bonds.

The term “(C₂-C₆)alkynyl” refers to straight or branched carbon chains with one or more triple bonds wherein the number of atoms is in the range 2 to 6.

The term “(C₃-C_(y))heterocycloalkyl(C₁-C_(x))alkyl” refers to the above “(C_(r) C_(x))alkyl” group wherein one or more hydrogen atoms are replaced by one or more “(C₃-C_(y))heterocycloalkyl” groups.

As used herein, the expression “ring system” refers to mono- or bicyclic ring systems which may be saturated, partially unsaturated or unsaturated, such as aryl, (C₃-C₈)cycloalkyl, (C₃-C₇)heterocycloalkyl or heteroaryl, having 5 to 11 ring atoms in which at least one ring atom is a heteroatom (e.g. N, S or O).

The expression “aryl” refers to mono or bi-ring systems which have 6 to 10 ring atoms, wherein at least one ring is aromatic.

The expression “heteroaryl” refers to mono or bi-ring systems with 5 to 11 ring atoms, in which at least one ring is aromatic and in which at least one ring atom is a heteroatom (e.g. N, NH, S or O).

Examples of suitable aryl or 5 or 6-membered heteroaryl monocyclic systems include, for instance, phenyl, thiophene (thiophenyl), benzene (phenyl), pyrrole (pyrrolyl), pyrazole (pyrazolyl), imidazole (imidazolyl), isoxazole (isoxazolyl), oxazole (oxazolyl), isothiazole (isothiazolyl), thiazole (thiazolyl), pyridine (pyridinyl), imidazolidine (imidazolidinyl), furan (furanyl) radicals and the like.

Examples of suitable aryl or heteroaryl bicyclic systems include naphthalene (naphthyl), biphenylene (biphenylenyl), purine (purinyl), pteridine (pteridinyl), benzotriazole (benzotriazolyl), quinoline (quinolinyl), isoquinoline (isoquinolinyl), indole (indolyl), isoindole (isoindolyl), benzothiophene (benzothiophenyl), dihydrobenzo dioxin, dihydrobenzo dioxepin, benzo oxazin radicals and the like.

Thus, the present invention is directed to a class of compounds acting as inhibitors of the phosphodiesterase 4 (PDE4) enzyme. Said class of compounds inhibits the conversion of cyclic nucleotides, in particular cyclic adenosine monophosphate (cAMP), into their inactive 5′-mononucleotide forms.

In the airways, the physiological responses to elevated intracellular levels of cyclic nucleotides, in particular of cAMP, lead to the suppression of the activity of immune and pro-inflammatory cells such as mast cells, macrophages, T lymphocytes, eosinophils and neutrophils, resulting in a decrease of the release of inflammatory mediators which include cytokines such as IL-1, IL-3 and tumor necrosis factor-alpha (TNF-α). It also leads to an airway smooth muscle relaxation and a decrease in oedema.

The present invention relates to derivatives of 1-phenyl-2-pyridinyl alkyl alcohols of general formula (I), N-oxides on the pyridine ring and pharmaceutically acceptable salts or solvates thereof:

wherein R₁, R₂, R₃, R₁₉, Z, A and K are as above defined.

It will be apparent to those skilled in the art that compounds of general formula (I) contain at least one stereogenic center, namely represented by the carbon atom (1) with an asterisk below, and therefore exist as optical stereoisomers.

When the compounds according to the invention have at least one stereogenic center, they may accordingly exist as enantiomers. When the compounds according to the invention possess two or more stereogenic centers, they may additionally exist as diastereoisomers. It is to be understood that all such isomers and mixtures thereof in any proportion are encompassed within the scope of the present invention.

In a preferred embodiment, the present invention is directed to compounds of formula (I)′, which are compounds of formula (I) as above defined where the absolute configuration of carbon (1) is that shown below:

The absolute configuration for carbon (1) is assigned on the basis of Cahn-Ingold-Prelog nomenclature based on groups' priorities.

In one preferred embodiment, for compounds of formula (I), the absolute configuration at carbon (1) is (S).

When the compounds of formula (I) possess a second stereogenic center, namely at carbon (2) represented by another asterisk herebelow, they exist as at least four diastereoisomers:

The four diastereoisomers thereof are represented below:

and are comprised within the scope of the present invention.

In a preferred embodiment, the present invention is directed to compounds of formula (I)″, which are compounds of formula (I)′ as above defined where the absolute configuration of carbon (2) is that shown below:

In another preferred embodiment, the present invention is directed to compounds of formula (I)′″, which are compounds of formula (I)′ as above defined where the absolute configuration of carbon (2) is that shown below:

For compounds of formula (I)″ and (I)′″, the absolute configuration of carbon (1) and (2) is assigned on the basis of Cahn-Ingold-Prelog nomenclature based on groups' priorities.

It is to be understood that all preferred groups or embodiments described herebelow and hereabove for compounds of formula (I) may be combined among each other and apply to compounds of formula (IG), (IL), (I)′, (I)″, (I)′″, (I)″″ and (I)′″″ as well mutatis mutandis.

In a preferred embodiment, the invention provides compounds of formula (IH), which are N-oxides derivatives of the pyridine ring of compounds of formula (I), or pharmaceutically acceptable salts thereof:

In a preferred embodiment, 2-pyridinyl ring has two R₃ substituents which are halogen atom. In a further preferred embodiment, such R₃ substituents are two chlorine atoms at positions 3 and 5 of the pyridine ring.

In one preferred embodiment, R₁ is (C₁-C₆)haloalkyl or (C₁-C₆)alkyl.

In one preferred embodiment, R₂ is (C₁-C₆)alkyl which optionally is substituted by (C₃-C₇)cycloalkyl or is a (C₃-C₇)cycloalkyl.

In another preferred embodiment, R₁ and R₂, together with the interconnecting atoms, form a 2,2-difluoro-1,3-dioxolane ring of formula (q) fused to the phenyl moiety which bears groups OR₁ and —OR₂, wherein asterisks indicate carbon atoms shared with such phenyl ring:

In a further preferred embodiment, R₁ is (C₁-C₆)haloalkyl and R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl.

In another preferred embodiment, R₁ is (C₁-C₆)alkyl and R₂ is (C₁-C₆)alkyl.

In a preferred embodiment, R₁₉ is hydrogen.

In a further preferred embodiment, R₁₉ is hydrogen, R₁ is (C₁-C₆)haloalkyl and R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl.

In another preferred embodiment, R₁₉, if different from hydrogen, forms together with R₂ a group of formula (x) wherein bonds labeled with (1) and (2) indicate the points of attachment for group (x) to atoms bearing groups R₁₉ and R₂ respectively

in such a way that R₂ and R₁₉ together with the interconnecting atoms form a ring of formula (w) which is fused to phenyl ring which bears groups —OR₂ and R₁₉, wherein asterisks indicate carbon atoms shared with such phenyl ring:

A preferred group of compounds of general formula (I) is that wherein the 2-pyridinyl ring is substituted in positions 3 and 5 with two atoms of chlorine, according to the general formula (IA):

wherein R₁, R₂, R₁₉, K, z, and A are as defined above for compounds of formula (I); and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

Another preferred group of compounds of formula (I) is that shown below according to general formula (IB):

wherein R₃, K, Z and A are as defined above for compounds of formula (I); and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

A further preferred group of compounds of formula (I) is that shown below according to general formula (IC):

wherein K, Z and A are as defined above for compounds of formula (I); and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

In one preferred embodiment, A is a (C₃-C₇)heterocycloalkyl-ene group comprising a nitrogen atom which represents the connecting point to group K as below represented:

In another preferred embodiment, A is selected in the list of di-radicals below reported:

wherein the symbols [3] and [4] indicate the points of connection for group A with, respectively, groups Z and K.

In a further preferred embodiment, A is selected in the list of di-radicals below reported:

wherein the symbols [3] and [4] indicate the points of connection for group A with, respectively, groups Z and K.

In an additional preferred embodiment, A is a group

wherein the symbols [3] and [4] indicate the points of connection for group A with, respectively, groups Z and K.

In a preferred embodiment, Z is a group —(CH₂)_(n)— in which n is zero.

Another preferred group of compounds of formula (I) is that shown below according to general formula (ID):

wherein R₁, R₂, R₃ and K are as defined above for compounds of formula (I), R₁₉ is hydrogen, Z is a bond (i.e., n is zero), and A is a thiazolidine divalent radical group as above represented; and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

Another preferred group of compounds of formula (I) is that shown below according to general formula (ID′″):

wherein R₁, R₂, R₃ and K are as defined above for compounds of formula (I), R₁₉ is hydrogen, Z is a bond (i.e. n is zero), A is a thiazolidine divalent radical group and stereogenic center have absolute configuration as above represented; and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

In one embodiment, for compounds of formula (ID) or (ID′″), R₁ is (C₁-C₆) haloalkyl, R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl, 2-pyridinyl ring is substituted in positions 3 and 5 with two chlorine R₃ groups, and K is a group

Another preferred group of compounds of formula (I) is that shown below according to general formula (IE):

wherein R₁, R₂, R₃ and K are as defined above for compounds of formula (I), Z is a bond (i.e. n is zero), R₁₉ is hydrogen and A is a pyrrolidine divalent radical group as above represented; and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

Another preferred group of compounds of formula (I) is that shown below according to general formula (IE′″):

wherein R₁, R₂, R₃ and K are as defined above for compounds of formula (I), Z is a bond (i.e. n is zero), R19 is hydrogen, A is a pyrrolidine divalent radical group, and the stereogenic centers have the absolute configuration as above represented; and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

In one embodiment, for compounds of formula (IE) or (IE′″), R₁ is (C₁-C₆)haloalkyl, R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl, 2-pyridinyl ring is substituted in 3 and 5 with two chlorine R₃ groups, and K is a group

In one preferred embodiment, K is selected in the list of groups below reported:

wherein the symbol [5] indicates the point of connection for group K with group A.

In another preferred embodiment, K is selected in the list of groups below reported:

wherein the symbol [5] indicates the point of connection for group K with group A.

In yet another preferred embodiment, K is selected in the list of groups below reported:

wherein the symbol [5] indicates the point of connection for group K with group A.

In further preferred embodiment, K is a group

wherein the symbol [5] indicates the point of connection for group K with group A.

In a preferred embodiment, R₄ is selected in the group consisting of: a group phenyl, a 5 or 6-membered heteroaryl group, a monocyclic (C₃-C₇)heterocycloalkyl and a bicyclic ring system; and each of which is optionally substituted by one or more groups R₅.

In one preferred embodiment, R₄ is a group phenyl or a 5 or 6-membered heteroaryl group, each of which is optionally substituted by one or more groups R₅.

In a further preferred embodiment, R₄ is a group phenyl which is optionally substituted by one or more groups R₅.

In a still preferred embodiment, R₄ is a 5 or 6-membered heteroaryl group which is optionally substituted by one or more groups R₅.

In another preferred embodiment, R₄ is a monocyclic (C₃-C₇)heterocycloalkyl optionally substituted by one or more groups R₅.

In a still preferred embodiment, R₄ is a bicyclic ring system optionally substituted by one or more groups R₅.

In one preferred embodiment, the number of substituents R₅ is zero, 1, or 2. In a further preferred embodiment, such number is 1.

In one preferred embodiment, R₅ is independently selected in the group consisting of:

-   -   —(C₁-C₆)alkyl optionally substituted by one or more groups         independently selected in the list consisting of:         (C₃-C₇)cycloalkyl, —OH and a group —NR₁₈C(O)(C₁-C₄)alkyl,         wherein R₁₈ is hydrogen or (C₁-C₄)alkyl-(C₃-C₇)heterocycloalkyl;     -   5 or 6-membered heteroaryl which is optionally substituted by         one or two groups (C₁-C₄)alkyl;     -   (C₁-C₆)haloalkyl;     -   (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;     -   a group —OR₆ wherein R₆ is selected from the group consisting         of:         -   (C₁-C₆)haloalkyl;         -   (C₁-C₁₀)alkyl optionally substituted by one or more             (C₃-C₇)cycloalkyl;     -   a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl;     -   halogen atoms;     -   cyano;     -   NR₈R₉ wherein R₈ and R₉ are different or the same and are         independently selected from the group consisting of:         -   H;         -   (C₁-C₆)alkyl, optionally substituted with (C₃-C₇)cycloalkyl,             (C₃-C₇)heterocycloalkyl;         -   a group —SO₂R₁₅, wherein R₁₅ is (C₁-C₄)alkyl;         -   or they form with the nitrogen atom to which they are linked             a saturated or partially saturated heterocyclic ring, which             is optionally substituted by one or more (C₁-C₆)alkyl or oxo             groups;     -   (C₁-C₄)alkylene-NR₈R₉;     -   COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl;     -   oxo;     -   —SO₂R₁₁ wherein R₁₁ is NR₈R₉ wherein R₈ and R₉ are as defined         above;     -   —COOR₁₂ wherein R₁₂ is H or (C₁-C₄)alkyl or         (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined above;         and     -   —CONR₈R₉ wherein R₈ and R₉ are as defined above.

In another preferred embodiment, R₅ is independently selected in the group consisting of:

-   -   (C₁-C₆)alkyl;     -   (C₃-C₇)heterocycloalkyl;     -   (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;     -   a group —OR₆ wherein R₆ is selected from the group consisting         of:         -   (C₁-C₆)haloalkyl;         -   —(C₁-C₁₀)alkyl optionally substituted by one or more             (C₃-C₇)cycloalkyl;     -   a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl;     -   halogen atoms;     -   NR₈R₉ wherein R₈ and R₉ are different or the same and are         independently selected from the group consisting of:         -   H;         -   (C₁-C₆)alkyl, optionally substituted with (C₃-C₇)cycloalkyl,             (C₃-C₇)heterocycloalkyl;         -   a group —SO₂R₁₅, wherein R₁₅ is (C₁-C₄)alkyl;         -   or they form with the nitrogen atom to which they are linked             a saturated or partially saturated heterocyclic ring, which             is optionally substituted by one or more (C₁-C₆)alkyl or oxo             groups;     -   —(C₁-C₄)alkylene-NR₈R₉;     -   COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl;     -   oxo;     -   —SO₂R₁₁ wherein R₁₁ is NR₈R₉ wherein R₈ and R₉ are as defined         above;     -   —COOR₁₂ wherein R₁₂ is H or (C₁-C₄)alkyl or         (C₁-C₄)alkylene-NR₈R₉ wherein     -   R₈ and R₉ are as defined above; and     -   —CONR₈R₉ wherein R₈ and R₉ are as defined above.

In another preferred embodiment, R₅ is independently selected in the group consisting of:

-   -   (C₁-C₆)alkyl;     -   —(C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl;     -   a group —OR₆ wherein R₆ is (C₁-C₁₀)alkyl optionally substituted         by one or more (C₃-C₇)cycloalkyl;     -   halogen atoms;     -   NR₈R₉ wherein R₈ and R₉ are different or the same and are         independently selected from the group consisting of:         -   H;         -   —(C₁-C₆)alkyl, optionally substituted with             (C₃-C₇)cycloalkyl, (C₃-C₇)heterocycloalkyl;         -   a group —SO₂R₁₅, wherein R₁₅ is (C₁-C₄)alkyl; or they form             with the nitrogen atom to which they are linked a saturated             or partially saturated heterocyclic ring, which is             optionally substituted by (C₁-C₆)alkyl or oxo;     -   —COOR₁₂ wherein R₁₂ is H or (C₁-C₄)alkyl or         (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined above;         and     -   —CONR₈R₉ wherein R₈ and R₉ are as defined above.

In a further preferred embodiment, R₅ is selected in the group consisting of:

-   -   —(C₁-C₆)alkyl;     -   —NR₈R₉ wherein R₈ and R₉ are different or the same and are         independently selected from the group consisting of:         -   H;         -   —(C₁-C₆)alkyl; and     -   CONR₈R₉ wherein R₈ and R₉ are as defined above.

A further preferred group of compounds of formula (I) is that shown below according to general formula (IF):

wherein Z is a bond, R19 is hydrogen, A is a (C₃-C₇)heterocycloalkyl-ene group comprising a nitrogen atom which represents the connecting point to group K, K is selected in the list of groups consisting of:

R₄ is a group phenyl or a 5 or 6-membered heteroaryl group, each of which is optionally substituted by one or more groups R₅: and the corresponding N-oxide on the pyridine ring, or pharmaceutically acceptable salts thereof.

According to a preferred embodiment, the present invention provides the compounds reported below:

Compound Chemical Name 19 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-(cyclopropylmethoxy)-4- (methylsulfonamido)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 30 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(4-methoxy-3- (methylsulfonyloxy)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 53 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3,4- dimethoxyphenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 135 4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 142 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4- (methylsulfonamido)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 143 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4-(N-(2- morpholinoethyl)methylsulfonamido)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 151 4-((S)-2-((R)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 150 4-((S)-2-((S)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 136 4-((S)-2-((S)-1-(4-aminophenylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 15 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(1-((4-(methoxycarbonyl)-5-methylfuran-2- yl)methyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 124 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)-4- methoxyphenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 77 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-4-(3- sulfamoylphenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1- oxide or 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-4-(3- sulfamoylphenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1- oxide 144 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(2-oxo-2-(thiophen-2-yl)ethyl)thiazolidine- 2-carbonyloxy)ethyl)pyridine 1-oxide 16 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide or 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(4- (dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 17 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide or 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(4- (dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 26 4-((2S)-2-(3-(4-aminobenzoyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 56 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 80 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(4-(3- (dimethylcarbamoyl)phenylsulfonyl)thiomorpholine-3- carbonyloxy)ethyl)pyridine 1-oxide 81 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(4-(4-(N- methylsulfamoyl)phenylsulfonyl)thiomorpholine-3- carbonyloxy)ethyl)pyridine 1-oxide 137 4-((2S)-2-(3-(3-amino-4-methoxyphenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 57 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 138 4-((S)-2-((R)-3-(4-aminophenylsulfonyl)thiazolidine-4-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 139 4-((2S)-2-(4-(4-aminophenylsulfonyl)morpholine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 54 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 78 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(4-(3- (dimethylcarbamoyl)phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 84 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-4- carbonyloxy)ethyl)pyridine 1-oxide 58 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(1,3-dioxoisoindolin-5- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 125 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 55 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 59 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-sulfamoylphenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 122 4-((2S)-2-(3-(3-carboxy-4-methoxyphenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 60 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-fluorophenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 61 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(2,4-dimethylphenylsulfonyl)thiazolidine- 2-carbonyloxy)ethyl)pyridine 1-oxide 62 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(thiophen-2-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 123 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-(dimethylcarbamoyl)-4- methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 121 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-(4-(3- (dimethylcarbamoyl)phenylsulfonyl)piperazin-1-yl)acetoxy)ethyl)pyridine 1-oxide 126 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4-(4-methylpiperazine-1- carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 63 3,5-dichloro-4-((2S)-2-(3-(3-chlorophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 64 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(1-methyl-1H-imidazol-2- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 65 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(cyclopropylmethylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 66 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(pyridin-3-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 67 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(2,4-difluorophenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 68 3,5-dichloro-4-((2S)-2-(3-(2-chloro-4-fluorophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 69 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4-fluoro-2- methylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 70 3,5-dichloro-4-((2S)-2-(3-(2-chlorophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 71 3,5-dichloro-4-((2S)-2-(3-(cyclohexylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 72 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(2,4-dioxo-1,2,3,4-tetrahydroquinazolin-6- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 85 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(thiophen-3-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 52 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 82 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 83 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 49 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-(cyclopropylmethoxy)-5-(N-(2- morpholinoethyl)methylsulfonamido)benzoyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 73 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3,4- dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 141 (S)-4-(2-(2-(4-(4-aminophenylsulfonyl)piperazin-1-yl)acetoxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 129 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)-4- methoxyphenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide 74 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(6-morpholinopyridin-3- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 127 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4-methoxy-3-(4-methylpiperazine-1- carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 128 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4-methoxy-3-(morpholine-4- carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 31 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-methoxy-3- (morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide or 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(4-methoxy-3- (morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 32 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-(N,N-dimethylsulfamoyl)-4- methoxybenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 75 4-((S)-2-((S)-3-(3-carboxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2- (3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide or 4-((S)-2-((R)-3-(3-carboxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2- (3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 33 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4- (morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 79 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(4-(phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 76 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3,5-dimethylisoxazol-4- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 38 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(thiazole-5-carbonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 34 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3- ((dimethylamino)methyl)benzoyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 35 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(oxazole-5-carbonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 130 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-(4-methylpiperazine-1- carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 155 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2- ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 86 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 87 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(5-(methoxycarbonyl)thiophen-2- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 88 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(pyridin-3-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 131 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)-4- methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 89 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 90 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-1H-imidazol-2- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 91 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- sulfamoylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 92 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(4- (methylsulfonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 93 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3,4- dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 51 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(5-((dimethylamino)methyl)thiophene-2- carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 22 4-((2S)-2-(3-(4-(2-aminoethyl)benzoyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 94 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(N- methylsulfamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 95 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(furan-2-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 96 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(furan-3-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 97 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-(N,N- dimethylsulfamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 98 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3,4- dimethoxyphenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide 99 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(pyridin-3-ylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 100 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (methoxycarbonyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 101 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2- (methoxycarbonyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 102 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-4- carbonyloxy)ethyl)pyridine 1-oxide 103 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 104 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (trifluoromethoxy)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 36 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(1,1- dioxothiomorpholinobenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 37 4-((S)-2-((S)-3-(4-carbamoylbenzoyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 105 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(6-morpholinopyridin-3- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 20 4-((S)-2-((S)-3-(4-(aminomethyl)picolinoyl)thiazolidine-2-carbonyloxy)-2- (3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide or 4-((S)-2-((R)-3-(4-(aminomethyl)picolinoyl)thiazolidine-2-carbonyloxy)- 2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 106 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-methoxy-4- methylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 107 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2,4-dimethylthiazol-5- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 108 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-methyl-3,4-dihydro-2H- benzo[b][1,4]oxazin-6-ylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 42 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-picolinoylthiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 133 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-((2- morpholinoethoxy)carbonyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide or 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(3-((2- morpholinoethoxy)carbonyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 110 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 111 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(6-morpholinopyridin-3- ylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide 112 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(4-nitrophenylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 113 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-(N,N- dimethylsulfamoyl)phenylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 114 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)piperidine-2- carbonyloxy)ethyl)pyridine 1-oxide 115 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2,5- dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 116 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2- ylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide 117 4-((S)-2-((S)-3-(3-acetylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 39 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 40 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(1,1-dioxo thiomorpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 21 4-((S)-2-((S)-3-(3-(aminomethyl)benzoyl)thiazolidine-2-carbonyloxy)-2- (3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 41 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-(oxazol-5-yl)benzoyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 140 4-((S)-2-((S)-3-(3-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 109 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (methylsulfonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 132 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-(4-methylpiperazine-1- carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 118 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(3-(3-(N- methylsulfamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 119 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-1H-imidazol-4- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 188 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-phenylacetyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 189 3,5-dichloro-4-((S)-2-((S)-3-(2-cyclopropylacetyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 190 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (phenylsulfonyl)propanoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 191 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-morpholinopropanoyl)thiazolidine- 2-carbonyloxy)ethyl)pyridine 1-oxide 192 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-(4-methylpiperazin-1- yl)propanoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 193 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 194 4-((S)-2-(2-((S)-1-benzoylpyrrolidin-2-yl)acetoxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 195 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-((S)-1-(3- (dimethylcarbamoyl)benzoyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1- oxide 198 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-(3- (dimethylcarbamoyl)phenyl)acetyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 199 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(2-(3- (dimethylcarbamoyl)phenyl)acetyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 200 3,5-dichloro-4-((S)-2-((S)-3-(2-cyanophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 201 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2,3-dihydrobenzo[b][1,4]dioxin-6- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 202 3,5-dichloro-4-((S)-2-((S)-3-(2-cyano-5- methylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 203 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2,5-dimethylthiophen-3- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 204 4-((S)-2-((S)-3-(4-bromo-2-fluoro-5-methylphenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 205 4-((S)-2-((S)-3-(3-bromo-4-methylphenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 206 3,5-dichloro-4-((S)-2-((S)-3-(4-cyanophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 207 3,5-dichloro-4-((S)-2-((S)-3-(3-cyanophenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 208 4-((S)-2-((S)-3-(4-(1H-pyrazol-1-yl)phenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 209 3,5-dichloro-4-((S)-2-((S)-3-(3-cyano-4-fluorophenylsulfonyl)thiazolidine- 2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 210 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-2-oxoindolin-5- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 211 3,5-dichloro-4-((S)-2-((S)-3-(2-chloro-5-cyanophenylsulfonyl)thiazolidine- 2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 212 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(5-methylbenzo[b]thiophen-2- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 213 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(1-methyl-1H-pyrazol-3- yl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 214 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4- (difluoromethoxy)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 215 3,5-dichloro-4-((S)-2-((S)-3-(4-chloro-2- (trifluoromethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide 216 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(5-fluoro-2- methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 217 4-((S)-2-((S)-3-(benzo[b]thiophen-2-ylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 218 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-oxo-2,3-dihydrobenzo[d]oxazol-6- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 219 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(2-oxopyrrolidin-1- yl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 220 4-((S)-2-((S)-3-(1-acetyl-1,2,3,4-tetrahydroquinolin-6- ylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 221 4-((S)-2-((S)-3-(4-(2-acetamidoethyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide 222 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(4-(2,2,2- trifluoroethoxy)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 223 4-(2-((S)-3-(benzylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 224 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(phenethylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 225 4-((S)-2-((S)-1-(benzylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 226 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(R)-3-(1-methyl-2-oxoindolin-5- ylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide 227 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(R)-1-(phenylsulfonyl)piperidine-3- carbonyloxy)ethyl)pyridine 1-oxide 228 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(R)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)piperidine-3- carbonyloxy)ethyl)pyridine 1-oxide 229 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)piperidine-3- carbonyloxy)ethyl)pyridine 1-oxide 230 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)piperidine-3- carbonyloxy)ethyl)pyridine 1-oxide 231 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(R)-4-(phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 232 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(R)-4-(3- (dimethylcarbamoyl)phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 233 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-4-(phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 234 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-4-(3- (dimethylcarbamoyl)phenylsulfonyl)morpholine-2- carbonyloxy)ethyl)pyridine 1-oxide 235 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-((S)-1-(phenylsulfonyl)pyrrolidin-2- yl)acetoxy)ethyl)pyridine 1-oxide 236 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide 237 4-((S)-2-(2-((S)-1-(benzylsulfonyl)pyrrolidin-2-yl)acetoxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 255 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-oxo-2-phenylethyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 256 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(2-oxo-2-phenylethyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 257 4-((S)-2-((S)-1-benzylpyrrolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 258 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)benzyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 261 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)-2- oxoethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 262 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(2-(3-(dimethylcarbamoyl)phenyl)-2- oxoethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 264 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(cyclopropylmethyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 265 4-((S)-2-((S)-3-benzylthiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 266 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 267 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-phenethylthiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 268 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-((S)-1-(3- (dimethylcarbamoyl)benzyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide 269 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-ureidophenylsulfonyl)thiazolidine- 2-carbonyloxy)ethyl)pyridine 1-oxide 271 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 274 4-((2S)-2-(2-(3-benzoylthiazolidin-2-yl)acetoxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 275 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-(3-(3- (dimethylcarbamoyl)benzoyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1- oxide 278 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-(3-(phenylsulfonyl)thiazolidin-2- yl)acetoxy)ethyl)pyridine 1-oxide 279 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(2-(3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidin-2- yl)acetoxy)ethyl)pyridine 1-oxide 281 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(1-(3- (dimethylcarbamoyl)phenylsulfonyl)azetidine-3- carbonyloxy)ethyl)pyridine 1-oxide 282 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-(1-(phenylsulfonyl)azetidine-3- carbonyloxy)ethyl)pyridine 1-oxide 283 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)azetidine-2- carbonyloxy)ethyl)pyridine 1-oxide 284 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)azetidine-2- carbonyloxy)ethyl)pyridine 1-oxide 285 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-2-oxoindolin-5- ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 287 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2- morpholinoethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 288 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(2-(4-methylpiperazin-1- yl)ethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 291 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 292 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(2-phenylacetyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 295 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)benzylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 296 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)benzylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 299 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 300 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3- (phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 301 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2- ((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 302 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2- ((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 303 3,5-dichloro-4-((S)-2-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide OR 3,5-dichloro-4-((R)-2-(2,2- difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 305 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1- (phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 306 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 307 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2- ((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 308 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2- ((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 309 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-1- (phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 310 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 311 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-1- (phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 312 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 313 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-(1- (phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 314 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-(1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 315 3,5-dichloro-4-((S)-2-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide OR 3,5-dichloro-4-((R)-2-(2,2- difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 316 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′- cyclopentane]-7-yl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 317 3,5-dichloro-4-(2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(4- methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide 320 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 321 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3- (phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 322 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-3- (phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 323 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 324 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-3- (phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 325 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 326 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′- cyclopentane]-7-yl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 327 3,5-dichloro-4-(2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(4- methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide 238 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-(N,N- dimethylsulfamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 239 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3-methylisoxazolo[5,4-b]pyridin-5- ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 240 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(1,3-dimethyl-1H-pyrazolo[3,4- b]pyridin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 241 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-5-(methylcarbamoyl)-1H- pyrrol-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 242 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(5-(pyrrolidine-1-carbonyl)-1H-pyrrol- 3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 243 (S)-((S)-1-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3,5- dichloropyridin-4-yl)ethyl) 3-(1-methyl-1H-imidazol-2- ylsulfonyl)thiazolidine-2-carboxylate 328 4-((S)-2-((S)-3-(1H-1,2,4-triazol-5-ylsulfonyl)thiazolidine-2-carbonyloxy)- 2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 186 4-((S)-2-((S)-3-benzoylthiazolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 187 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 244 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-1-(phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 184 4-((S)-2-((R)-1-benzoylpyrrolidine-2-carbonyloxy)-2-(3- (cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5- dichloropyridine 1-oxide 185 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-1-(3- (dimethylcarbamoyl)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1- oxide 245 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 246 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3- (dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 247 (S)-((S)-1-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3,5- dichloropyridin-4-yl)ethyl) 3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylate 248 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 249 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 263 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)-2-((S)-3-(3- (dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 250 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(4-methyl-3,4-dihydro-2H- benzo[b][1,4]oxazin-6-ylsulfonyl)pyrrolidine-2- carbonyloxy)ethyl)pyridine 1-oxide 251 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-1-(3-methylisoxazolo[5,4-b]pyridin-5- ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide 252 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(4-methyl-3,4-dihydro-2H- benzo[b][1,4]oxazin-6-ylsulfonyl)thiazolidine-4- carbonyloxy)ethyl)pyridine 1-oxide 253 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((R)-3-(3-methylisoxazolo[5,4-b]pyridin-5- ylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide 254 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4- (difluoromethoxy)phenyl)-2-((S)-3-(3- (methylcarbamoyl)phenylsulfonyl)thiazolidine-2- carbonyloxy)ethyl)pyridine 1-oxide or pharmaceutically acceptable salts or solvates thereof.

In another preferred embodiment, the compounds of the invention are selected in the group consisting of:

-   4-((S)-2-((S)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(4-methylpiperazine-1-carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(pyridin-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-1H-imidazol-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-sulfamoylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(methylsulfonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3,4-dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(N,N-dimethylsulfamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(5-(pyrrolidine-1-carbonyl)-1H-pyrrol-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-5-(methylcarbamoyl)-1H-pyrrol-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-methylisoxazolo[5,4-b]pyridin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-ureidophenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-2-oxoindolin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine     1-oxide; -   3,5-dichloro-4-((S)-2-((S)-3-(4-cyanophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine     1-oxide;     and pharmaceutically acceptable salts or solvates thereof.

In one aspect of the present invention, a process for the preparation of compounds of the invention is provided, according to general synthetic routes reported in Scheme 1 below, where reference is made to specific synthetic schemes which are better detailed in the following paragraphs.

The processes which can be used and are described below and reported in Schemes, should not be viewed as limiting the scope of the synthetic methods available for the preparation of the compounds of the invention.

In the following Schemes, for compounds of formula (II) to (XIX), unless otherwise indicated, groups R₁ to R₂₀, Z, A, and K have the same meanings as described for compounds of formula (I) above.

Compounds of formula (Ia), i.e. compounds of formula (I) wherein K is a group —(CH₂)R₄, may be prepared according to Scheme 2a below by reaction of a compound of formula (II) wherein A′ is (C₃-C₇)heterocycloalkyl-ene group comprising a group —NH—, with an appropriate compound of formula (III).

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (III) in a suitable dipolar solvent, such as THF, methanol, ethanol or DCM, in the presence of an appropriate reducing agent, such as sodium triacetoxy borohydride, sodium cyano borohydride or sodium borohydride, and of an appropriate acid, such as acetic acid, HCl in methanol or ammonium acetate. It could be useful to preform the imine before adding the reducing agent. The reaction proceeds smoothly at room temperature (RT) over 1 to 12 hours.

Alternatively compounds of formula (Ia), i.e. compounds of formula (I) wherein K is a group —(CH₂)R₄, may be prepared according to Scheme 2b below by reaction of a compound of formula (II) wherein A′ is (C₃-C₇)heterocycloalkyl-ene group comprising a group —NH—, with an appropriate compound of formula (XVI).

Typical reaction conditions comprise reacting a compound of formula (XVI), where X is a leaving group such as Cl or Br, with a compound of formula (II) in a suitable polar aprotic solvent, such as acetonitrile or DMF, in the presence of an appropriate base such as K₂CO₃, alkaline bicarbonate, TEA or DIPEA, at a temperature ranging from RT to 70° C.

Compounds of formula (Ib), i.e. compounds of formula (I) wherein K is a group —C(O)(CH₂)_(j)R₄, may be prepared according to Scheme 3a below by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (IV).

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (IV) in a suitable dipolar aprotic solvent, such as DMF, chloroform or DCM, in the presence of an appropriate condensing agent such as EDC, DCC, HOBT, HOAT, or CDI, and, if necessary, of an appropriate agent, such as DMAP, HOBT, 4-pyrrolidinopyridine (4-PPY) or other 4-alkylamino pyridine, at room temperature.

Alternatively compounds of formula (Ib), i.e. compounds of formula (I) wherein K is a group —C(O)(CH₂)_(j)R₄, may be prepared according to Scheme 3b below by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (XVII).

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (XVII) in a suitable solvent such as pyridine or DCM, and in the presence, if necessary, of an appropriate base such as TEA, DIPEA, DBU, or another organic base at a temperature ranging from 0° C. to room temperature.

Compounds of formula (Ic), i.e. compounds of formula (I) wherein K is a group —(CH₂)_(m)C(O)R₄, may be prepared according to Scheme 4 below by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (V), where Hal represents a suitable halogen leaving group.

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (V) in a suitable polar aprotic solvent, such as DMF or acetonitrile, in the presence of an appropriate base such as K₂CO₃, alkaline bicarbonate, TEA or DIPEA, at a temperature ranging from RT to 50° C.

Compounds of formula (Id), i.e. compounds of formula (I) wherein K is a group —(CH₂)_(y)SO₂R₄, may be prepared according to Scheme 5 below by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (VI), where Hal represents a suitable halogen leaving group.

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (VI) in a suitable polar aprotic solvent such as DMF or acetonitrile, in the presence of an appropriate base such as K₂CO₃, alkaline bicarbonate, TEA, or DIPEA, at a temperature ranging from RT to 50° C.

Compounds of formula (Id), i.e. compounds of formula (I) wherein K is a group —(CH₂)_(y)SO₂R₄ and y is 1, may also be prepared according to Scheme 46 below by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (XVIII), where Hal represents a suitable halogen leaving group.

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (XVIII) in a suitable polar aprotic solvent, such as DMF or acetonitrile, in the presence of an appropriate base such as K₂CO₃, alkaline bicarbonate, TEA, or DIPEA, at a temperature ranging from RT to 50° C. Compound (XIX) thus obtained is successively reacted with a suitable oxidizing agent, such as MCPBA or hydrogen peroxide, in a suitable polar solvent, such as DCM, chloroform, EtOH or MeOH, at a temperature ranging from room temperature to 60° C. Compounds of formula (Ie), i.e. compounds of formula (I) wherein K is a group —SO₂(CH₂)_(p)R4, may be prepared according to Scheme 6 below reported by reaction of a compound of formula (II) as above defined, with an appropriate compound of formula (VII).

Typical reaction conditions comprise reacting a compound of formula (II) with a compound of formula (VII) in a suitable solvent such as pyridine or DCM, and in the presence, if necessary, of an appropriate base such as TEA, DIPEA, DBU, or another organic base at a temperature ranging from 0° C. to room temperature.

Alternatively, compounds of formula (I), may be prepared according to Scheme 7 below by reaction of a compound of formula (VIII), with an appropriate compound of formula (IX).

Typical reaction conditions comprise reacting a compound of formula (VIII) with a compound of formula (IX) in a suitable polar aprotic solvent, such as DMF, THF, chloroform, or DCM, in the presence of an appropriate condensing agent such as EDC, DCC, or CDI and of an appropriate agent, such as DMAP, HOBT, 4-pyrrolidinopyridine (4-PPY) or other 4-alkylamino pyridine at room temperature; removal of possibly present protecting group is performed under conditions known to the person skilled in the art or as described in ‘Protection Groups in Organic Synthesis’ by T. W. Green and P. Wutz, (Wiley-Interscience publication, 1999, which is incorporated herein by reference in its entirety).

Compounds of formula (II), as above defined, may be prepared according to Scheme 8 below by reaction of a compound of formula (X), wherein A″ is (C₃-C₇) heterocycloalkyl-ene group comprising a group —N— which is protected with a suitable protecting group, with an appropriate compound of formula (XI), followed by removal of N— protecting group under appropriate conditions.

Typical coupling reaction conditions comprise reacting a compound of formula (VIII) with a compound of formula (X) in a suitable polar aprotic solvent, such as DMF, THF, chloroform, or DCM, in the presence of an appropriate (coupling) condensing agent such as EDC, DCC, or CDI and of an appropriate agent such as DMAP, HOBT, 4-pyrrolidinopyridine (4-PPY) or other 4-alkylamino pyridine at room temperature; removal of protecting group is performed under conditions known to the person skilled in the art or as described in ‘Protection Groups in Organic Synthesis’ by T. W. Green and P. Wutz (Wiley-Interscience publication, 1999, which is incorporated herein by reference in its entirety), for example when the protecting group is represented by a t-butoxycarbonyl group then deprotection may be conveniently performed under acidic conditions (such as HCl in dioxane or in AcOEt or TFA in CH₂Cl₂).

Alternatively the corresponding acyl chloride can be preformed, by reacting compound (X) with oxalyl chloride or thionyl chloride or other reagents well known to those skilled in the art, in a suitable aprotic solvent such as DCM at 0 degrees, in presence, if necessary, of a catalytic amount of DMF, and successively adding compound (VIII) and an appropriate base such as TEA or DIPEA.

Compounds of formula (If), i.e. compounds of formula (I) wherein K is a group —SO₂(CH₂)_(p)R₄ and R₂ is hydrogen, may be prepared according to Scheme 42 below by reaction of a compound of formula (Ie) as above defined, wherein R₂ is (C₁-C₆)alkyl, optionally substituted by one (C₃-C₇)cycloalkyl under appropriate conditions.

Typical reaction conditions comprise reacting a compound of formula (Ie) as above defined with a suitable acid, such as TFA or BBr₃ or BCl₃, at a temperature ranging from room temperature to 40 degrees.

The N-oxides on the 2-pyridinyl ring of the compounds of general formula (I) and embodiments thereof may be prepared according to methods available in the literature and well known to the skilled person. For instance, they may be prepared by dissolving the compound of general formula (I) or embodiments thereof in CH₂Cl₂ or CHCl₃, then adding an oxidizing agent such as m-chloro perbenzoic acid (mCPBA) to the resulting solution. Other oxidizing agents which may be used are hydrogen peroxide, perbenzoic acid, and peracetic acid.

Alternatively, in particular for those compounds in which A or A′ is a ring substituted with a functional group sensitive to oxidation, the corresponding N-oxides are prepared by carrying out the oxidation step before further functional groups are introduced, for example on compounds of formula (II) or (VIII).

In a preferred embodiment, the process for preparation of compounds of formula (I) or embodiments thereof is performed starting from N-oxide on the pyridine ring of compound of formula (VIII), thus allowing the preparation of compound of formula (I) or embodiments thereof in the form of N-oxides on the pyridine ring. Compounds of general formula (III), (IV), (V), (VI), (VII), (VIII), (IX), (XVI), (XVII), (XVIII), (XIX), and (X) may be commercially available, their preparation may be specifically described in the literature or they may be prepared according to methods available in the literature and known to the person skilled in the art.

In particular, compounds of formula (VIII) and corresponding N-oxides on the pyridine ring may also be prepared as described in International Patent Application Nos. WO 2009/018909 or WO 2010/089107.

In one embodiment, a preferred process for the preparation of compounds of formula (IDa), i.e. N-oxide derivatives on pyridine ring of compounds of formula (ID) wherein R₉ is hydrogen, K is a group —SO₂(CH2)_(p)R₄ and wherein absolute configuration at the stereogenic centers is as below represented, is provided according to Scheme 43 below reported.

Typical reaction conditions for the process described in Scheme 43 comprise: a) adding a solution of a compound of formula (VII) in pyridine (3-30 vol. preferably 8 vol.) to a refrigerated solution of a compound of formula (XI), in pyridine (3-30 vol. preferably 8 vol.) stirring the resulting solution at room temperature; c) pouring the solution into aqueous HCl in excess; d) filtering the precipitated material and washing it with water, or d′) extracting the aqueous phase with AcOEt, washing with aqueous HCl M, brine and evaporating the resulting organic phase; and optionally e) dissolving the solid obtained from step d) or d′) in AcOEt, charging it on a silica gel pad, eluting with AcOEt/MeOH [100:0 to (90:10)] and evaporating under vacuum the resulting solution, or e′) purifying the product by flash cromathography eluting with DCM/i-PrOH.

In a more preferred embodiment, compounds of formula (IDa) obtained as above reported according to Scheme 43 are crystallized by a process comprising: dissolving the compounds in EtOH (8 vol); g) vigorously stirring overnight at room temperature; h) filtering the solid formed; and, optionally, i) washing the solid obtained from step h) with EtOH (2 vol) and 1) drying the solid under vacuum.

In a further preferred embodiment, step 1) of Scheme 43 is conducted by drying first the solid under vacuum at room temperature, followed by drying under vacuum at 60° C.

In one embodiment, a preferred process is provided for the preparation of compounds of formula (XI) as above defined, according to Scheme 44 below reported:

Typical reaction conditions for the process described in Scheme 44 comprise: a) adding under stirring a solution of conc. HCl (about 5M; large excess) in dry AcOEt (9 vol.) to a solution of a compound of formula (XII) in AcOEt (6 vol.) at room temperature; b) stirring; c) filtering the precipitated solid; optionally d) washing the obtained solid with AcOEt; and optionally e) drying the solid obtained under vacuum at room temperature.

In one embodiment, a preferred process is provided for the preparation of compounds of formula (XII) as above defined, according to Scheme 45 below reported:

Typical reaction conditions for the process described in Scheme 45 comprise: a) adding a compound of formula (XIV), DMAP, and EDC to a solution of a compound of formula (XV) in DMF; b) stirring the mixture, preferably overnight; c) pouring the mixture into cold water; d) filtering the precipitate; optionally e) dissolving the precipitate in DCM, washing the solution with water, drying and evaporating the solvent; and optionally f) dissolving the solid obtained from step d) or e) in boiling MTBE (3.5 vol.) adding petroleum ether (4 vol.) under stirring, stirring at room temperature, filtering the solid obtained and drying it at room temperature under vacuum.

In a preferred embodiment, processes according to schemes 43, 44, and 45 are sequentially performed to obtain crystalline compounds of formula (IDa).

In a preferred embodiment, a process is provided for the preparation of compounds of formula (IDaa), i.e. a compound of formula (IDa) wherein R₁ is (C₁-C₆) haloalkyl, R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl, 2-pyridinyl ring is substituted in 3 and 5 with two chlorine R₃ groups, K is a group

and R₄ is a phenyl group which is optionally substituted by one or more groups R₅; which process comprises sequentially performing reactions as provided in Schemes 43, 44, and 45 above described.

In one aspect of the present invention, compounds of formula (II), their N-oxides on the pyridine ring, or salts thereof are provided as intermediates in the process for the preparation of compounds of formula (I)

wherein A′ is (C₃-C₇)heterocycloalkyl-ene group comprising a group —NH—.

In one embodiment, compounds of formula (XI) as above defined are provided as intermediates in the process of preparation of compounds of formula (IDa). In a further preferred embodiment, for compounds of formula (XI), R₁ is (C₁-C₆)haloalkyl and R₂ is (C₁-C₆)alkyl which is substituted by (C₃-C₇)cycloalkyl, and the pyridine ring is substituted by two groups R₃ placed at position 3 and 5.

In another aspect of the present invention, compounds of formula (II) as above defined are provided which act as inhibitors of the phosphodiesterase 4 (PDE4) enzyme, thus solving the above mentioned need of identifying further PDE4 inhibitors endowed with a high affinity for PDE4 enzyme, and possibly showing an appropriate developability profile as an inhalation treatment for example in terms of reduced side effects.

Also provided by the present invention are compositions containing compounds of formula (II) and therapeutic uses thereof.

Where applicable, preferred embodiments and groups described above for compounds of formula (I), apply to compounds of formula (II) as well mutatis mutandis.

The process described is particularly advantageous as it is susceptible of being properly modulated, through any proper variant known to the skilled person, so as to obtain any of the desired compounds of the invention. Such variants are comprised within the scope of the present invention.

From all of the above, it should be clear to the skilled person that any of the described groups may be present as such or in any properly protected form. In particular, functional groups present in the compounds of formula (II), (III), (IV), (V), (VI), (VII), (VIII), (IX), (X), (XI), (XII), (XIII), (XIV), (XV), (XVI), (XVII), (XVIII), and (XIX) and which could generate unwanted side reaction and by-products, need to be properly protected before the alkylation, acylation, coupling, oxidation, or sulfonylation takes place. Likewise, subsequent deprotection of those same protected groups may follow upon completion of the said reactions.

In the present invention, unless otherwise indicated, the term “protecting group” designates a protective group adapted to preserve the function of the group it is bound to. Typically, protective groups are used to preserve amino, hydroxyl, or carboxyl functions. Appropriate protecting groups may thus include, for example, benzyl, benzyloxycarbonyl, t-butoxycarbonyl, alkyl, or benzyl esters or the like, which are well known to those skilled in the art (see, for a general reference, T. W. Green; Protective Groups in Organic Synthesis (Wiley, N.Y. 1999) which is incorporated herein by reference in its entirety). Likewise, selective protection and deprotection of any of the said groups, for instance including carbonyl, hydroxyl, or amino groups, may be accomplished according to very well known methods commonly employed in organic synthetic chemistry.

Optional salification of the compounds of formula (I) or N-oxides on the pyridine ring thereof may be carried out by properly converting any of the free acidic or amino groups into the corresponding pharmaceutically acceptable salts. In this case too, the operative conditions being employed for the optional salification of the compounds of the invention are all within the ordinary knowledge of the skilled person.

From all of the above, it should be clear to the skilled person that the above processes, comprehensive of any variant thereof for the preparation of suitable compounds of the invention, may be conveniently modified so that to adapt the reaction conditions to the specific needs, for instance by choosing appropriate condensing agents, solvents and protective groups, as the case may be.

The present invention also provides pharmaceutical compositions of compounds of the invention or of compounds of formula (II) in admixture with one or more pharmaceutically acceptable carriers, for example those described in Remington's Pharmaceutical Sciences Handbook, XVII Ed., Mack Pub., N.Y., U.S.A., which is incorporated herein by reference in its entirety.

Administration of the compounds of the present invention or of compounds of formula (II) may be accomplished according to patient needs, for example, orally, nasally, parenterally (subcutaneously, intravenously, intramuscularly, intrasternally, and by infusion), by inhalation, rectally, vaginally, topically, locally, transdermally, and by ocular administration. Various solid oral dosage forms may be used for administering compounds of the present invention including such solid forms as tablets, gelcaps, capsules, caplets, granules, lozenges, and bulk powders. The compounds of the present invention or compounds of formula (II) may be administered alone or combined with various pharmaceutically acceptable carriers, diluents (such as sucrose, mannitol, lactose, starches) and excipients known in the art, including but not limited to suspending agents, solubilizers, buffering agents, binders, disintegrants, preservatives, colorants, flavorants, lubricants, and the like. Time release capsules, tablets, and gels are also advantageous in administering the compounds of the present invention or compounds of formula (II).

Various liquid oral dosage forms may also be used for administering compounds of the present invention or compounds of formula (II), including aqueous and non-aqueous solutions, emulsions, suspensions, syrups, and elixirs. Such dosage forms can also contain suitable inert diluents known in the art such as water and suitable excipients known in the art such as preservatives, wetting agents, sweeteners, flavorants, as well as agents for emulsifying and/or suspending the compounds of the invention or compounds of formula (II). The compounds of the present invention or compounds of formula (II) may be injected, for example, intravenously, in the form of an isotonic sterile solution. Other preparations are also possible.

Suppositories for rectal administration of the compounds of the present invention or of compounds of formula (II) may be prepared by mixing the compound with a suitable excipient such as cocoa butter, salicylates, and polyethylene glycols. Formulations for vaginal administration may be in the form of cream, gel, paste, foam, or spray formula containing, in addition to the active ingredient, such suitable carriers as are known in the art.

For topical administration the pharmaceutical composition may be in the form of creams, ointments, liniments, lotions, emulsions, suspensions, gels, solutions, pastes, powders, sprays, and drops suitable for administration to the skin, eye, ear, or nose. Topical administration may also involve transdermal administration via means such as transdermal patches.

For the treatment of the diseases of the respiratory tract, the compounds according to the present invention or compounds of formula (II) are preferably administered by inhalation. Inhalable preparations include inhalable powders, propellant-containing metering aerosols, and propellant-free inhalable formulations.

For administration as a dry powder, single- or multi-dose inhalers known from the prior art may be utilized. In that case the powder may be filled in gelatine, plastic, or other capsules, cartridges, or blister packs or in a reservoir.

A diluent or carrier, generally non-toxic and chemically inert to the compounds of the invention, e.g. lactose or any other additive suitable for improving the respirable fraction may be added to the powdered compounds of the invention or compounds of formula (II).

Inhalation aerosols containing propellant gas such as hydrofluoroalkanes may contain the compounds of the invention or compounds of formula (II) either in solution or in dispersed form. The propellant-driven formulations may also contain other ingredients such as co-solvents, stabilizers, and optionally other excipients.

The propellant-free inhalable formulations comprising the compounds of the present invention or compounds of formula (II) may be in form of solutions or suspensions in an aqueous, alcoholic, or hydroalcoholic medium and they may be delivered by jet or ultrasonic nebulizers known from the prior art or by soft-mist nebulizers such as Respimat®.

The compounds of the present invention or compounds of formula (II) may be administered as the sole active agent or in combination with other pharmaceutical active ingredients including those currently used in the treatment of respiratory disorders, e.g. beta2-agonists, antimuscarinic agents, corticosteroids, mitogen-activated protein kinases (P38 MAP kinase) inhibitors, nuclear factor kappa-B kinase subunit beta (IKK2) inhibitors, human neutrophil elastase (FINE) inhibitors, phosphodiesterase 4 (PDE4) inhibitors, leukotriene modulators, non-steroidal anti-inflammatory agents (NSAIDs), and mucus regulators.

The present invention also provides combinations of a compound of the present invention or of compounds of formula (II), with a β2-agonist selected from the group consisting of carmoterol, GSK-642444, indacaterol, milveterol, arformoterol, formoterol, salbutamol, levalbuterol, terbutaline, AZD-3199, BI-1744-CL, LAS-100977, bambuterol, isoproterenol, procaterol, clenbuterol, reproterol, fenoterol and ASF-1020, and salts thereof.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a corticosteroid selected from the group consisting of fluticasone propionate, fluticasone furoate, mometasone furoate, beclometasone dipropionate, ciclesonide, budesonide, GSK 685698, and GSK 870086.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with an antimuscarinic agent selected from the group consisting of aclidinium, tiotropium, ipratropium, trospium, glycopyrronium, and oxitropium salts.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a PDE4 inhibitor selected from the group consisting of AN-2728, AN-2898, CBS-3595, apremilast, ELB-353, KF-66490, K-34, LAS-37779, IBFB-211913, AWD-12-281, cipamfylline, cilomilast, roflumilast, BAY19-8004 and SCH-351591, AN-6415, indus-82010, TP1-PD3, ELB-353, CC-11050, GSK-256066, oglemilast, OX-914, tetomilast, MEM-1414, and RPL-554.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a P38 MAP kinase inhibitor selected from the group consisting of semapimod, talmapimod, pirfenidone, PH-797804, GSK-725, minokine, and losmapimod and salts thereof.

In a preferred embodiment, the present invention provides combinations of a compound of the present invention or of a compound of formula (II) with an IKK2 inhibitor.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a HNE inhibitor selected from the group consisting of AAT, ADC-7828, Aeriva, TAPI, AE-3763, KRP-109, AX-9657, POL-6014, AER-002, AGTC-0106, respriva, AZD-9668, zemaira, AAT IV, PGX-100, elafin, SPHD-400, prolastin C, and prolastin inhaled.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a leukotriene modulator selected from the group consisting of montelukast, zafirlukast, and pranlukast.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a NSAID selected from the group consisting of ibuprofen and ketoprofen.

The present invention also provides combinations of a compound of the present invention or of a compound of formula (II), with a mucus regulator selected from the group consisting of INS-37217, diquafosol, sibenadet, CS-003, talnetant, DNK-333, MSI-1956, and gefitinib.

The dosages of the compounds of the present invention depend upon a variety of factors including the particular disease to be treated, the severity of the symptoms, the route of administration, the frequency of the dosage interval, the particular compound utilized, the efficacy, toxicology profile, and pharmacokinetic profile of the compound.

Advantageously, the compounds of the present invention or compounds of formula (II) may be administered for example, at a dosage comprised between 0.001 and 1000 mg/day, preferably between 0.1 and 500 mg/day.

When they are administered by inhalation route, the dosage of the compounds of the present invention or of compounds of formula (II) is advantageously comprised between 0.01 and 20 mg/day, preferably between 0.1 and 10 mg/day.

Preferably, the compounds of the present invention or compounds of formula (II) alone or combined with other active ingredients may be administered for the prevention and/or treatment of any obstructive respiratory disease such as asthma, chronic bronchitis, and chronic obstructive pulmonary disease (COPD).

However the compounds of the present invention or compounds of formula (II) may be administered for the prevention and/or treatment of any disease wherein PDE4 inhibition is required. Said disease include: allergic disease states such as atopic dermatitis, urticaria, allergic rhinitis, allergic conjunctivitis, vernal conjunctivitis, eosinophilic granuloma, psoriasis, inflammatory arthritis, rheumatoid arthritis, septic shock, ulcerative colitis, Crohn's disease, reperfusion injury of the myocardium and brain, chronic glomerulonephritis, endotoxic shock, cystic fibrosis, arterial restenosis, artherosclerosis, keratosis, rheumatoid spondylitis, osteoarthritis, pyresis, diabetes mellitus, pneumoconiosis, toxic and allergic contact eczema, atopic eczema, seborrheic eczema, lichen simplex, sunburn, pruritus in the anogenital area, alopecia greata, hypertrophic scars, discoid lupus erythematosus, systemic lupus erythematosus, follicular and wide-area pyodermias, endogenous and exogenous acne, acne rosacea, Beghet's disease, anaphylactoid purpura nephritis, inflammatory bowel disease, leukemia, multiple sclerosis, gastrointestinal diseases, autoimmune diseases and the like.

Such diseases also include neurological and psychiatric disorders such as Alzheimer's disease, multiple sclerosis, amylolaterosclerosis (ALS), multiple systems atrophy (MSA), schizophrenia, Parkinson's disease, Huntington's disease, Pick's disease, depression, stroke, and spinal cord injury.

Other features of the invention will become apparent in the course of the following descriptions of exemplary embodiments which are given for illustration of the invention and are not intended to be limiting thereof.

EXAMPLES

Chemical names of the compounds were generated with Structure To Name Enterprise 10.0 Cambridge Software.

Abbreviations.

EDC=1-ethyl-3-(3-dimethylaminopropyl) carbodiimide) hydrochloride; DMAP=4-dimethylaminopyridine; DMF=dimethylformamide; EtOAc or AcOEt=Ethyl acetate; RT=room temperature; THF=tetrahydrofurane; DCM=dichloromethane; Et₂O=diethyl ether; MeOH=methylic alcohol; n-BuOH=n-butylic alcohol; EtOH=ethyl alcohol; IprOH or IPA=isopropyl alcohol; (Ipr)₂O=diisopropylether; MIK=methyl isobutyl ketone; MEK=methyl ethyl ketone; MTBE=methyl tert-butyl ether; AcOH=acetic acid; vv=volumes; v/w=ratio volume/weight; and w/w=ratio weight/weight.

General Experimental Details. NMR Characterization:

¹H-NMR spectra were recorded on a 400 MHz Varian AS400 spectrometer. Chemical shift are reported as 6 values in ppm relative to trimethyl silane (TMS) as an internal standard. Coupling constants (J values) are given in hertz (Hz) and multiplicities are reported using the following abbreviation (s=singlet, d=doublet, t=triplet, q=quartet, m=multiplet, b r=broad, nd=not determined).

or

1H-NMR spectra were recorded on a Bruker ARX300 Spectrometer at 300.13 MHz (1H) using deuterated solvents, such as deuterated dimethylsulfoxide (DMSO-d6) or deuterated chloroform (CDCl₃). The instrument was equipped with a multinuclear inverse probe and temperature controller. Chemical shifts are expressed in parts per million (ppm) downfield of tetramethylsilane (d units). Multiplicity is indicated as follow: (s) singlet, (d) doublet, (dd) double doublet, (ddd) triple doublet, (t) triplet, (dt) double triplet, (q) quartet, (m) multiplet, (br s) broad signal. Coupling constants J are expressed in units of hertz (Hz).

LC/UV/MS Analytical Methods

LC/MS retention times are estimated to be affected by an experimental error of ±0.5 min.

LC/UV/MS—Method 1

LC instrument: HPLC Alliance Waters (or equivalent)

Column: Kinetex 2.6 u C18 100 A 100×4.6 mm (Phenomenex) Column Temperature (° C.): 50.0

Mobile phases: HCOONH4 0.025M pH3 (A); Acetonitrile (B) Flow (ml/min): 2.0 (split in MS 1:10) Stop Time (mins): 17.0

Gradient:

Time (min) % A % B 0.00 80.0 20.0 10.00 20.0 80.0 12.00 20.0 80.0 14.00 80.0 20.0 17.00 80.0 20.0 UV detection: channel 1 245 nm; channel 2 254 nm

Injection Volume (ul): 5.00 Sample Solvent Acetonitrile

MS instrument: Waters Quattro Micro API (or equivalent)

Polarity ES+ Capillary (kV) 3.20 Cone (V) 20.00 Extractor (V) 2.00 RF Lens (V) 0.3 Polarity ES− Capillary (kV) 3.20 Cone (V) 20.00 Extractor (V) 3.00 RF Lens (V) 0.3 Source Temperature (° C.) 110 Desolvation Temperature (° C.) 210 Cone Gas Flow (L/Hr) 150 Desolvation Gas Flow (L/Hr) 650 Scan duration (secs): 1.00 Interscan delay (secs): 0.10 Mass range: 125 to 1000

LC/UV/MS—Method 2

LC instrument: Acquity Waters HPLC (or equivalent)

Column: Kinetex 1.7 u XB-C18 100 A 100×2.1 mm (Phenomenex) Column Temperature (° C.) 50.0

Mobile phases: HCOONH₄ 0.025M pH3 (A); Acetonitrile+0.1% Formic Acid (B) Flow (ml/min) 0.65 (split in MS 1:3) Stop Time (mins) 10.0

Gradient:

Time (min) % A % B 0.00 80.0 20.0 5.50 20.0 80.0 7.50 20.0 80.0 8.00 80.0 20.0 10.00 80.0 20.0 UV detection: wavelength 254 nm Injection Volume (ul)—2.00 Sample solvents: Acetonitrile MS instrument: Waters ZQ (or equivalent)

Polarity ES+ Capillary (kV) 3.00 Cone (V) 20.00 Extractor (V) 3.00 RF Lens (V) 1.0 Polarity ES− Capillary (kV) 3.00 Cone (V) 20.00 Extractor (V) 3.00 RF Lens (V) 1.0 Source Temperature (° C.) 110 Desolvation Temperature (° C.) 210 Cone Gas Flow (L/Hr) 150 Desolvation Gas Flow (L/Hr) 650 Mass range: 100 to 950 Scan time (sec): 0.32

LC/UV/MS—Method 3

LC instrument: Acquity Waters HPLC (or equivalent) interfaced with 2996 PDA detector

Column: Acquity HPLC BEH C18 1.7 um 50×2.1 mm Column Temperature (° C.) 40.0

Mobile phases: 95:5 H2O:ACN+(0.1% TFA) (A); 5:95 H2O:ACN+(0.1% TFA) (B) Flow (ml/min) 0.6 (split in MS 1:6) Stop Time (mins) 8.5

Gradient:

Time (min) % A % B 0.00 95.0 5.0 0.50 95.0 5.0 6.00 0.0 100.0 7.00 0.0 100.0 7.10 95.0 5.0 8.50 95.0 5.0 UV detection: BPI Detection (Start Wavelength nm 210, End Wavelength nm 400, Sampling Rate spectra/sec=20) Injection Volume (ul)—1.00 Sample solvents: DMSO:MeOH:ACN ratio 1:3:3 MS instrument: Waters ZQ (or equivalent)

Polarity ES+ Capillary (kV) 3.20 Cone (V) 25.00 Extractor (V) 3.00 RF Lens (V) 0.1 Polarity ES− Capillary (kV) 3.00 Cone (V) 20.00 Extractor (V) 3.00 RF Lens (V) 0.3 Source Temperature (° C.) 150 Desolvation Temperature (° C.) 350 Cone Gas Flow (L/Hr) 110 Desolvation Gas Flow (L/Hr) 800 Mass range: 60 to 1200 Scan time (sec): 0.4

LC/UV/MS—Method 4

LC instrument: Acquity Waters HPLC (or equivalent) interfaced with 2996 PDA detector

Column: Kinetex C18 1.7 um 50×2.1 mm (Phenomenex) Column Temperature (° C.): 40.0

Mobile phases: 95:5 H₂O:ACN+(0.1% TFA) (A); 5:95 H₂O:ACN+(0.1% TFA) (B) Flow (ml/min): 0.5 (no split in MS) Stop Time (mins): 4.40

Gradient:

Time (min) % A % B 0.00 95.0 5.0 0.30 95.0 5.0 3.30 0.0 100.0 3.90 0.0 100.0 4.40 95.0 5.0 UV detection: BPI Detection (Start Wavelength nm 200, End Wavelength nm 400, Sampling Rate points/sec=20)

Injection Volume (ul): 4.00 Sample Solvent Acetonitrile

MS instrument: ZQ (or equivalent)

Polarity ES+ Capillary (kV) 3.25 Cone (V) 27.00 Extractor (V) 3.00 RF Lens (V) 0.4 Source Temperature (° C.) 120 Desolvation Temperature (° C.) 400 Cone Gas Flow (L/Hr) 100 Desolvation Gas Flow (L/Hr) 800 Scan time (sec): 0.42 Mass range: 100 to 800

Preparative REVERSE-PHASE HPLC Conditions Preparative HPLC—Method 1

Waters Micromass ZQ/Sample manager 2767 Photodiode array detector 2996;

Column: XTerra Prep MS C18 Column (5 μm, 19×150 mm, Waters)

Flow rate: 20 ml/min with MS detection UV wavelength: 254 nm. Mobile phase: Solvent A (water:MeCN:HCOOH 95:5:0.05); Solvent B (water:MeCN:HCOOH 5:95:0.05)

Gradient:

Time (min) % A % B 0.00 100.0 0.00 1.00 100 0.00 10.00 0.00 100.0 11.00 0.00 100.0 12.00 100.0 0.00

Preparative HPLC—Method 2 Column: Waters Symmetry Prep C18 17 um 19×300

Flow: 20 ml/min Mobile phase: 90% H₂O, 10% acetonitrile, 0.05% TFA (A); 10% H₂O, 90% acetonitrile, 0.05% TFA (B)

Gradient:

Time (min) % A % B 0.00 95 5 2.5 95 5 22 0 100 30 0 100

Preparative HPLC—Method 3

Waters Micromass ZQ/sample manager 2767 Photodiode array detector: 2996

Column: XTERRA Prep MS C18 10 um 19×300

Flow: 20 ml/min Mobile phases: H₂O, 0.1% TFA (A); acetonitrile, 0.1% TFA (B)

Gradient:

Time (min) % A % B 0.00 90 10 2 90 10 23 0 100 30 0 100

Conditioning:

Time (min) % A % B 30.5 90 10 32 90 10

Chiral HLPC:

The enantiomeric purity was determined on Hewlett Packard 1050 HPLC system using Chiracel OD column (5μ 4.6×250 mm), eluting using isocratic mixture of hexane and isopropanol in different ratios as indicated in each specific example.

Flow=0.8 ml/min UV detection=230 nm.

Optical Rotation (Activity) Determination

Specific rotations of compounds were measured with a Polarimeter Perkin Elmer model 241 or 341.

Temperature (° C.) 25 Path Length (dm)  1 Wavelength Sodium D-line (589 nm) Experiments requiring microwave heating were performed using a Biotage Initiator Sixty instrument.

Procedures for Salt Formation

Unless otherwise stated, salts described in the experimental section were obtained according to one of the procedures herebelow described:

Formate Salts: when stated in the Salt Name column, compounds containing one or more basic centres and purified by reverse-phase HPLC (Method 1) were obtained as formic acid salts, once clean fractions collected form chromatography were evaporated under reduced pressure without any further basic treatment.

Trifluoroacetate Salts: when stated in the Salt Name column, compounds containing one or more basic centres and purified by reverse-phase HPLC (Method 2 or 3) were obtained as 2,2,2-trifluoroacetic acid salts, once clean fractions collected from chromatography were evaporated under reduced pressure without any further basic treatment.

Hydrochloride Salts: when stated in the Salt Name column, Compounds containing one or more basic centres which underwent Boc deprotection under acidic condition without any further basic work-up, were obtained as hydrochloride salts.

Any other salt was obtained treating the base with a solution of the corresponding acid under conditions know to the skilled person.

The salt stoichiometry was determined, if required, by NMR.

In the procedures that follow, after each starting material, reference to a compound number is typically provided. This is provided merely for assistance to the skilled chemist. The starting material may not necessarily have been prepared from the batch referred to.

When reference is made to the use of a “similar” or “analogous” procedure, as will be appreciated by those skilled in the art, such a procedure may involve minor variations, for example reaction temperature, reagent/solvent amount, reaction time, work-up conditions or chromatographic purification conditions. Stereogenic centers which are indicated by an undefined line bond, represent those in compounds which were obtained as single diastereisomers or enantiomers but whose absolute configuration was anyway not determined.

Many of the Compounds described in the following Examples have been prepared from sterochemically pure starting materials, for example 95% ee.

The stereochemistry of the compounds in the Examples, where indicated, has been assigned on the assumption that the absolute configuration at resolved stereogenic centers of staring materials is maintained throughout any subsequent reaction conditions. The absolute configuration for some of the Compounds described has been confirmed as correct by X-ray or VCD (Vibrational Circular Dichroism) analysis of crystalline material.

Diastereoisomeric ratio by LC/UV/MS, when indicated, is estimated to be affected by an experimental error of ±1%. Alternatively diastereoisomeric ratio is determined by ¹H NMRand it is estimated to be >95:5 when a single diastereoisomer was detected using NMR analysis.

Detailed synthetic pathways and procedures for specific examples are outlined in Schemes 9-41 and 46 herebelow. The synthesis of alcohol intermediates listed in Table 12 is described in the listed patent applications, all of which are incorporated herein by reference in their entireties.

TABLE 12 Entry Structure Preparation  1

Prepared as described in patent WO 2010/089107 156

Prepared as described in patent WO 2009/018909 157

Prepared as described in patent WO 2009/018909 158

Prepared as described in patent WO 2010/089107 159

Prepared as described in patent WO 2010/089107 160

Prepared as described in patent WO 2009/018909

The intermediates used in the procedures described below are commercially available, obtainable by the skilled person through synthetic approaches well known in the art, or obtainable following the synthetic procedures described in the Examples below.

Example 17 (S)-3,5-dichloro-4-(2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide 164)

Step 1: 4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(3-(cyclopropyl-methoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (161)

A mixture of (S)-2-acetoxy-2-phenylacetic acid (0.924 g, 4.76 mmol), (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (1.0 g, 2.380 mmol), EDC (0.684 g, 3.57 mmol), and DMAP (0.436 g, 3.57 mmol) in DCM (150 ml) was stirred at RT for 24 hours. More (S)-2-acetoxy-2-phenylacetic acid (0.350 g, 1.802 mmol), EDC (0.456 g, 2.380 mmol), and DMAP (0.300 g, 2.456 mmol) were added and the stirring was continued for 3 hours to complete conversion. The reaction mixture was washed twice with aqueous 1N HCl and then with aqueous 1M K₂CO₃; the organic layer was dried over Na₂SO₄ and evaporated to dryness. The residue was triturated with iPrOH (30 ml) and filtered to afford the desired product (1.27 g, 2.129 mmol, 89% yield). MS/ESI⁺ 596.18 [MH]⁺

Step 2: 4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (162)

4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (1.27 g, 2.129 mmol) was treated with trifluoroacetic acid (15 ml, 195 mmol), and the resulting solution was stirred at RT for 20 hours. The reaction mixture was diluted with DCM and washed twice with water; the organic layer was dried over Na₂SO₄ and evaporated to dryness. The residue was purified by chromatography on silica gel (DCM/EtOAc=3:2 to 1:1). The mixed fractions were combined and triturated with a mixture of iPr₂O/Et₂O (10:1). The collected solid was then combined to pure fractions from chromatography to afford the desired compound (1.08 g, 1.991 mmol, 94% yield); MS/ESI⁺ 542.11 [MH]⁺

¹H NMR (300 MHz, DMSO-d6) δ ppm 8.56 (s, 2H), 7.27-7.50 (m, 5H), 6.98 (d, 1H), 6.81 (d, 1H), 7.00 (t, 1H), 6.54 (dd, 1H), 5.89 (dd, 1H), 5.84 (s, 1H), 3.40 (dd, 1H), 3.18 (dd, 1H), 2.13 (s, 3H)

Step 3: 4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(4-(difluoromethoxy)-3-methoxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (163)

A suspension of 4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (1.080 g, 1.991 mmol), methyl iodide (0.162 ml, 2.59 mmol), and potassium carbonate (0.550 g, 3.98 mmol) in CH₃CN (40 ml) was vigorously stirred at RT for 20 hours. The reaction mixture was partitioned between DCM and water and the organic layer was dried over Na₂SO₄. The solvent was removed under vacuum to afford the desired compound (0.984 g, 1.769 mmol, 89% yield). MS/ESI⁺ 556.17 [MH]⁺. The raw compound was used without further purification.

Step 4: (S)-3,5-dichloro-4-(2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (164)

4-((S)-2-((S)-2-acetoxy-2-phenylacetoxy)-2-(4-(difluoromethoxy)-3-methoxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (984 mg, 1.769 mmol) was dissolved in a mixture of MeOH (50 ml) and DCM (10 ml). Aqueous sat. NaHCO₃ solution (10 ml, 11.00 mmol) was added, and the resulting suspension was stirred at RT for 2 hours. The reaction mixture was partitioned between water and DCM; the organic layer was dried over Na₂SO₄ and evaporated to dryness to afford the desired compound (650 mg, 1.71 mmol, 97% yield). MS/ESI⁺ 380.03 [MH].

The compound listed in Table 13 was prepared with an analogous procedure to that described in Scheme 23, by using suitable alkylation reagent and performing Step 3 at 65° C.

TABLE 13 MS/ESI⁺ Entry Structure [MH] 165

610.24

Example 18 Synthesis of (S)-3,5-dichloro-4-(2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (170)

Step 1: Synthesis of 2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxyphenyl)ethanol (166)

3,5-dichloro-4-methylpyridine (160) (54 g, 331 mmol) was dissolved in dry THF (480 mL) under anargon atmosphere and it was cooled at −78° C. in dry-ice/acetone bath. LHMDS 1N THF solution (331 ml, 331 mmol) was added drop-wise by keeping the temperature at −78°. The mixture was stirred at −78° for 1 hour. After that, a solution of 3,4-dimethoxybenzaldehyde (50 g, 301 mmol) in dry THF (120 ml) was added drop-wise by keeping the temperature at −78° C. When the addition was completed, the mixture was allowed to warm at RT.

The reaction was poured in ice and water (1 L), and the mixture was stirred until a copious precipitate formed. The solid was filtered, and dissolved in ethyl acetate (500 ml), dried over Na₂SO₄ and the solvent evaporated under vacuum. The crude was crystallized in CHCl₃/hexane. The precipitate was filtered, washed with hexane and dried under vacuum at 40° C. for 8 hours to give 55 g (yield 45%). The mother liquor solution was evaporated under vacuum at 40° C., dissolved in ethyl acetate (200 ml) and extracted with 200 ml of water. The organic solution was dried over Na₂SO₄ and the solvent evaporated under vacuum at 40° C. The crude was crystallized in CHCl₃/hexane, and additional 15 g of the desired product (166) were obtained (overall yield 70%).

Step 2: Synthesis of ((R)-2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxyphenyl)ethyl) 2-(6-methoxynaphthalen-2-yl)propanoate (167)

Intermediate 166 (50 g, 152 mmol), (R)-2-(6-methoxynaphthalen-2-yl)propanoic acid (38.6 g, 168 mmol), DMAP (20.5 g, 168 mmol), and EDC (43.8 g, 229 mmol) were dissolved in DMF (300 ml), and the reaction mixture was stirred at RT for 2 hours. After that time water (500 ml) was added, and the solution stirred upon precipitation occurs. The solid was filtered and dissolved in DCM (500 ml). The organic solution was washed with aqueous HCl 1N (2×500 ml), saturated aqueous NaHCO₃ solution (500 ml) and dried over Na₂SO₄. The solvent was evaporated under vacuum and the solid residue sonicated in EtOH (300 ml) and triturated for 1 hour. The resulting precipitate was collected by filtration and dried under vacuum at 40° C. for 4 hours to give 79 g (yield 99%) of compound 167, as diastereoisomeric mixture.

Step 3: Synthesis of (R)-((S)-2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxyphenyl)ethyl) 2-(6-methoxynaphthalen-2-yl)propanoate (168)

Intermediate 167 (79 g, 146 mmol) was dissolved in CHCl₃ (100 ml), and MeOH (30 ml) was slowly added up to persistent opalescence and the mixture lewft at RT for 2 hours. The solid formed was collected by filtration and re-crystallized by CHCl₃/MeOH (70 ml/20 ml) solvent system to obtain 35 g of compound 168 (yield 88%, ee 98%). Chiral HPLC analysis Rt=42.33 min (fast isomer); eluent: hexane:isopropanol 97:3 ¹H NMR (600 MHz, CHLOROFORM-d) δ ppm 8.04 (s, 2H), 7.67 (d, J=8.79 Hz, 1H), 7.58 (d, J=8.52 Hz, 1H), 7.53 (m, 1H), 7.12-7.20 (m, 3H), 6.95 (dd, J=8.24, 1.92 Hz, 1 H), 6.78-6.88 (m, 2H), 6.14 (dd, J=10.44, 4.12 Hz, 1H), 3.95 (s, 3H), 3.88 (s, 3H), 3.78-3.81 (m, 4H), 3.55 (dd, J=13.73, 10.44 Hz, 1H), 3.14 (dd, J=13.60, 4.26 Hz, 1H), 1.44 (d, J=7.14 Hz, 3H).

Step 4: Synthesis of (S)-2-(3,5-dichloropyridin-4-yl)-1-(3,4-dimethoxyphenyl)ethanol (169)

Intermediate 168 (30 g, 56 mmol) was dissolved in MeOH, and toluene was slowly added. Potassium terbutoxide was slowly added to the suspension. The mixture was stirred for 24 hours at RT. The reaction was diluted with water (500 ml), and the aqueous mixture was extracted with CHCl₃ (500 ml). The organic layer was dried over Na₂SO₄ and the solvent was evaporated under vacuum. The residue was crystallized from CHCl₃ (100 ml) and hexane (20 ml, till persistent opalescence). The mother liquor was concentrated and recrystallized in the same way giving a second crop of desired compound. Totally 16 g of compound 169 (yield 87%) were obtained.

Chiral HPLC analysis R_(t)=58.03 min; eluent:hexane:isopropanol 95:5. [α]_(D) ²⁰=+10.21 (c=0.506, methanol)

¹H NMR (400 MHz, acetone) δ ppm 8.47 (s, 2H), 6.96-7.15 (m, 1H), 6.87 (m, 2H), 4.93-5.21 (m, 1H), 4.50 (d, J=3.97 Hz, 1H), 3.78 (s, 6H), 3.44 (dd, J=12.79, 8.38 Hz, 1H), 3.22 (dd, J=13.01, 5.51 Hz, 1H).

MS/ESI⁺ [MH]⁺: 328.19

Step 5: Synthesis of (S)-3,5-dichloro-4-(2-(3,4-dimethoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (170)

Compound 169 (4 g, 12 mmol) was dissolved in ethyl acetate, and m-CPB acid was added to the solution. The mixture was stirred at RT for 5 hours. The formed solid was collected by filtration, washed with ethyl acetate and dried under vacuum to give 1.72 g of title compound (yield 41%).Chiral HPLC analysis Rt=22.16 min; eluent: hexane:isopropanol 6:4. [α]_(D) ²⁰=+68.91 (c=0.253, Methanol/CHCl₃ 1:1). MS/ESI⁺ [MH]⁺: 344.19

¹H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.15 (s, 2H), 6.99 (m, 1H), 6.79-6.88 (m, 2H), 5.03 (dd, J=8.50, 5.32 Hz, 1H), 3.75-3.98 (m, 6H), 3.42 (dd, J=13.57, 8.56 Hz, 1H), 3.19 (dd, J=13.51, 5.32 Hz, 1H), 2.06-2.15 (m, 1H).

Example 36 Synthesis of 3,5-dichloro-4-(2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)-2-hydroxyethyl)pyridine 1-oxide (172)

Step 1: Synthesis of 2-(3,5-dichloropyridin-4-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)ethanol (171)

3,5-dichloro-4-methylpyridine (166) (4.37 g, 0.016 mol) was dissolved in dry THF (40 mL) under an argon atmosphere and it was cooled at −78° C. in dry-ice/acetone bath. LHMDS IN THF solution (28 ml, 28 mmol) was added drop-wise by keeping the temperature at −78°. The mixture was stirred at −78° for 1 hour. After that, a solution of 2,3-difluoro-3,4-benzodioxolocarboxaldheyde (5 g, 0.026 mol) in dry THF (10 ml) was added drop-wise by keeping the temperature at −78° C. When the addition was completed, the mixture was allowed to warm at RT. The reaction was poured in ice and water, and the aqueous phase extracted with ethyl acetate (3×). The combined organic phases were dried over Na₂SO₄ and the solvent evaporated under vacuum. The crude was crystallized in petroleum ether/hexane 1/1. The precipitate was filtered, washed with hexane and dried under vacuum at 40° C. for 8 h to give 6.4 g (yield 45%).

MS/ESI⁺ 349.14 [MH]⁺; ¹H NMR (200 MHz, CHLOROFORM-d) δ ppm 8.71 (s, 2H), 7.48-7.68 (m, 2H), 6.85-7.07 (m, 1H), 4.61 (m, 1H), 4.11-4.44 (m, 2H).

Step 2: Synthesis of 3,5-dichloro-4-(2-(2,2-dimethylbenzo[d][1,3]dioxol-5-yl)-2-hydroxyethyl)pyridine 1-oxide (172)

2-(3,5-dichloropyridin-4-yl)-1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)ethanol (2 g, 5.74 mmol) was dissolved in EtOAc (40 ml), and the solution was cooled to 0° C. m-CPBA (5.29 g, 22.98 mmol) was added, and the resulting mixture was stirred at RT for 24 hours. The reaction mixture was cooled to 0° C., and the white solid precipitate was filtered and washed twice with cold DCM to afford the desired product (1.738 g, 4.77 mmol, 83%); MS/ESI⁺ 364.03 [MH]⁺

Example 19 Synthesis of 3,5-dichloro-4-(2-hydroxy-2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide (174)

Step 1: 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-'7-yl)-2-oxoethyl)pyridine 1-oxide (173)

To a solution of 2-(3,5-dichloropyridin-4-yl)-1-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethanone, (prepared as described in EP 1 535 920, which is incorporated herein by reference in its entirety, 4.75 g, 12.05 mmol) in EtOAc (125 ml) cooled at 0° C., m-CPBA (11.09 g, 48.2 mmol) was added and the reaction mixture was stirred at RT for 24 hours. More m-CPBA (5.54 g, 24.10 mmol) was added, and the stirring was continued for additional 24 hours. The mixture was washed several times with aqueous 1M K₂CO₃ and the organic layer was dried over Na₂SO₄ and evaporated to dryness. The residue was purified by chromatography on silica gel, (DCM/EtOAc=3/1 to 1/2) to afford 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)-2-oxoethyl)pyridine 1-oxide (2.14 g, 5.22 mmol, 43.3% yield); MS/ESI⁺ 410.10 [MH]⁺.

Step 2: 3,5-dichloro-4-(2-hydroxy-2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide (174)

To a solution of 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)-2-oxoethyl)pyridine 1-oxide (2.14 g, 5.22 mmol) in MeOH (100 ml), solid sodium borohydride (0.197 g, 5.22 mmol) was added portion-wise, and the mixture was stirred at RT overnight. Additional sodium borohydride (0.394 g, 10.44 mmol) was added and over 2 hours, and the stirring was continued for further 12 hours. The mixture was concentrated under vacuum, diluted with EtOAc, and washed twice with aqueous 1N NaOH. The organic layer was dried over Na₂SO₄, the solvent was removed under reduced pressure, and the residue was purified by chromatography on silica gel (EtOAc) to afford 3,5-dichloro-4-(2-hydroxy-2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide (650 mg, 1.577 mmol, 30.2% yield); MS/ESI⁺ 412.10 [MH]⁺.

Example 1 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-pyrrolidine-2 carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (3)

Step 1: 4-((S)-2-((S)-1-(tert-butoxycarbonyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (2)

(S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (1) (550 mg, 1.309 mmol), (S)-1-(tert-butoxycarbonyl)pyrrolidine-2-carboxylic acid (282 mg, 1.309 mmol), EDC (251 mg, 1.309 mmol), and DMAP (160 mg, 1.309 mmol) were dissolved in DMF (5 ml). The reaction was stirred at RT for 48 hours to achieve completion. After that time, the reaction was quenched with HCl 1M and extracted with EtOAc. The organic extract was washed with HCl 1M (×3) and with K₂CO₃ 5% (×3) before being dried over Na₂SO₄ and concentrated under vacuum to yield 800 mg of desired product (yield 99%). MS/ESI⁺ 617.16 [MH]⁺

Step 2: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (3) 4-((S)-2-((S)-1-(tert-butoxycarbonyppyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (2) (300 mg, 0.486 mmol) was dissolved in Dioxane/HCl (4M, 2 ml) and stirred at RT for 8 hours. After that time, the solvent was removed on a rotavapour under reduced pressure and dried in a vacuum oven overnight to yield the wanted product as an hydrochloride salt (200 mg; yield 80%).

MS/ESI⁺ 517.2 [MH]⁺; t_(R)/min (Methods 1)=3.75; Diastereomeric Ratio=>99:1; [α_(D)]=−32.80 (c=0.25; CHCl₃)

¹H NMR (400 MHz, METHANOL-d₄) S ppm 8.49 (s, 2H), 7.18 (d, J=7.94 Hz, 1H), 7.11 (d, J=1.76 Hz, 1H), 7.04 (d, J=1.76 Hz, 1H), 6.78 (t, J=75.00 Hz, 1H), 6.10-6.17 (m, 1H), 4.38-4.51 (m, 1H), 3.85-3.99 (m, 2H), 3.66 (m, 2H), 3.39-3.51 (m, 1H), 2.40-2.60 (m, 1H), 1.89-2.17 (m, 4H), 1.15-1.36 (m, 1H), 0.64 (dd, J=7.94, 1.32 Hz, 2H), 0.33-0.47 (m, 2H).

The compounds listed in Table 2 were prepared with an analogous procedure to that described in Example 1, by using suitable starting materials.

Compounds obtained as free bases underwent a basic work-up in place of removal of the solvent under reduced pressure described above (Ex: NaHCO₃ saturated solution), followed by extraction with polar organic solvent (Ex: AcOEt) in order to remove the salification with HCl, which spontaneously occurs performing Step 2 (Scheme 9).

Compound 6, 7, 181, and 183 were obtained by reacting its appropriate Boc-protected precursor with AcOEt/HCl (5M), followed by filtration at room temperature of the hydrochloride salt, which spontaneously precipitates from the reaction mixture. Compounds 177, 178, and 179 were obtained by performing Step 2 with HCl in EtOAc and removing the solvent without heating.

TABLE 1 HPLC-MS characterization t_(R)/min Entry Structure SALT NAME MS/ESI⁺ [MH]⁺ Methods 1 or 2 Distaereomeric Ratio ¹H NMR [α]_(D) 4

Free base 517.2 5

Free base 535.2 3.19; 3.26 (2)  40:60 6

hydrochloride 535.2 3.26 (2) 99:1 ¹H NMR (400 MHz, DMSO-d₆) δppm 8.57 (s, 2 H), 7.19 (d, J = 7.94 Hz, 1 H), 7.12 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.93- 7.00 (m, 1 H), 5.89-5.98 (m, 1 H), 5.12 (s, 1 H), 3.91 (d, J = 7.06 Hz, 2 H), 3.37-3.47 (m, 1 H), 3.10-3.31 (m, 3 H), 2.77-2.93 (m, 2 H), 1.05-1.36 (m, 1 H), 0.51-0.63 (m, 2 H), 0.34 (d, J = 4.85 Hz, 2 H). 7

Hydrochloride 535.2 8

Free base 533.2 1.86; 1.90 (2) 64:36 9

hydrochloride 531.2 2.03 (2) 97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.96- 9.18 (bs, 1 H), 8.80-8.96 (bs, 1 H), 8.62 (s, 2 H), 7.22 (d, J = 8.38 Hz, 1 H), 7.18 (d, J = 1.76 Hz, 1 H), 7.02-7.10 (m, 2 H), 6.12 (dd, J = 9.48, 4.63 Hz, 1 H), 4.16 (m, 1 H), 3.94 (dd, J = 7.06, 1.32 Hz, 2 H), 3.49-3.62 (m, 1 H), 3.17-3.34 (m, 3 H), 2.76-2.95 (m, 1 H), 2.04-2.17 (m, 1 H), 1.69 (d, J = 4.85 Hz, 2 H), 1.38-1.60 (m, 2 H), 1.23 (d, J = 3.53 Hz, 1 H), 0.51-0.66 (m, 2 H), 0.31-0.45 (m, 2 H). −10.83 (c = 0.48; CHCl₃) 10

hydrochloride 531.2 11

Free base 535.2 3.19 (2) 99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.04-7.13 (m, 2 H), 6.97 (dd, J = 8.16, 1.54 Hz, 1 H), 5.88-6.03 (m, 1 H), 3.97-4.15 (m, 3 H), 3.90 (d, J = 7.06 Hz, 2 H), 3.43 (dd, J = 14.11, 9.26 Hz, 1 H), 3.24 (dd, J = 14.11, 4.85 Hz, 1 H), 3.08 (dd, J = 10.14, 7.06 Hz, 1 H), 2.80 (dd, J = 10.14, 5.73 Hz, 1 H), 1.14-1.28 (m, 1 H), 0.48-0.67 (m, 2 H), 0.26-0.46 (m, 2 H). −45.77 (c = 0.48; CHCl₃) 12

hydrochloride 535.2 13

Free base 548.6 14

Bis hydrochloride 545.1 1H NMR (400 MHz, DMSO-d₆) δ ppm 8.89 (bs, 3 H), 8.58 (s, 2 H), 7.19 (d, J = 7.94 Hz, 1 H), 7.07-7.14 (m, 2 H), 6.98 (dd, J = 8.38, 1.76 Hz, 1 H), 6.00 (dd, J = 9.04, 4.63 Hz, 1 H), 3.90-3.92 (d, 2 H), 3.45 (dd, J = 14.11, 9.26 Hz, 1 H), 3.34 (s, 2H), 3.25 (dd, J = 14.11, 4.85 Hz, 1 H), 3.09 (m, 4 H), 2.80 (m, 4 H), 1.12- 1.32 (m, 1 H), 0.52-0.66 (m, 2 H), 0.27- 0.44 (m, 2 H) 175

hydrochloride 531.2 1.86 (Method 4) >95:5 ¹H NMR ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.87 (br. s., 2 H), 8.56 (s, 2 H), 7.19 (d, 1 H), 7.09 (d, 1 H), 6.97 (dd, 1 H), 7.07 (t, 1 H), 5.94 (dd, 1 H), 3.91 (d, 2 H), 3.46 (dd, 1 H), 3.28- 3.38 (m, 1 H), 3.23 (dd, 1 H), 3.09-3.19 (m, 1 H), 2.69-3.00 (m, 3 H), 1.90-2.11 (m, 1 H), 1.41-1.84 (m, 3 H), 1.09-1.30 (m, 1 H), 0.49-0.65 (m, 2 H), 0.30-0.42 (m, 2H) 176

hydrochloride 531.2 1.84 (Method 4) >95:5 ¹H NMR ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.97- 9.15 (m, 1 H), 8.81-8.97 (m, 1 H), 8.57 (s, 2 H), 7.20 (d, 1 H), 7.11 (d, 1 H), 7.00 (dd, 1 H), 7.08 (t, 1 H), 5.99 (dd, 1 H), 3.93 (d, 2H), 3.49 (dd, 1 H), 3.28-3.37 (m, 1 H), 3.22 (dd, 1 H), 3.07-3.18 (m, 1 H), 2.69-3.00 (m, 3 H), 1.85-2.06 (m, 1 H), 1.60-1.85 (m, 2 H), 1.37-1.60 (m, 1 H), 1.01-1.32 (m, 1 H), 0.47-0.74 (m, 2 H), 0.19-0.47 (m, 2 H) 177

hydrochloride 533.1 1.78 (Method 4) >95:5 ¹H NMR ¹H NMR (300 MHz, DMSO-d₆) δ ppm 9.45 (br. s., 1 H), 9.35 (br. s., 1 H), 8.55 (s, 2 H), 7.19 (d, 1 H), 7.10 (d, 1 H), 6.98 (dd, 1 H), 7.08 (t, 1 H), 5.99 (dd, 1 H), 4.52 (dd, 1 H), 3.98 (ddd, 1 H), 3.91 (d, 2 H), 3.79 (ddd, 1 H), 3.50 (dd, 1 H), 3.35-3.44 (m, 1 H), 3.25 (dd, 1 H), 2.88-3.21 (m, 3 H), 1.07-1.31 (m, 1 H), 0.47-0.77 (m, 2 H), 0.15-0.45 (m, 2H) 178

hydrochloride 533.0 1.78 (Method 4) >95:5 ¹H NMR ¹H NMR (300 MHz, DMSO-d₆) δ ppm 9.65- 10.08 (m, 1 H), 9.36-9.65 (m, 1 H), 8.55 (s, 2 H), 7.19 (d, 1 H), 7.11 (d, 1 H), 6.98 (dd, 1 H), 7.08 (t, 1 H), 5.98 (dd, 1 H), 4.53 (dd, 1 H), 3.96-4.07 (m, 1 H), 3.92 (d, 2 H), 3.82 (ddd, 1 H), 3.49 (dd, 1 H), 3.38-3.47 (m, 1 H), 3.26 (dd, 1 H), 3.10-3.21 (m, 1 H), 2.87- 3.11 (m, 2 H), 1.12-1.32 (m, 1 H), 0.49- 0.68 (m, 2 H), 0.15-0.49 (m, 2 H) 179

hydrochloride 531.11 180

Free base 517.2 1.92 (2) 98:2 181

Hydrochloride salt 535.2 182

Free base 517.2 1.99 (2) 98:2 183

Hydrochloride salt 535.2

Example 2 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-((4-(methoxycarbonyl)-5-methylfuran-2-yl)methyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (15)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (3) (40 mg, 0.077 mmol) was dissolved in THF (1 ml), and methyl 5-formyl-2-methylfuran-3-carboxylate (13.00 mg, 0.077 mmol) and acetic acid (4.64 mg, 0.077 mmol) were added to it. The reaction was stirred at RT for 30 minutes before adding sodium triacetoxyhydroborate (16.39 mg, 0.077 mmol). After that time, the reaction was stirred for further 2 hours to get to completion. The solvent was removed, and the residue was partitioned between EtOAc and aq HCl 1M. The organic layer was then washed with aq K₂CO₃ 5% and dried over Na₂SO₄. The solvent was removed under vacuum to obtain a transparent oil (35 mg; yield 68%) that was purified by preparative HPLC to yield 18 mg of diasteromeric mixture (47.5:52.5) of the desired product as transparent oil (yield 36%). MS/ESI⁺ 668.9 [MH]⁺; t_(R)=5.97; 6.15 min (Methodl); Diastereomeric Ratio=47:53.

The compounds listed in Table 3 were prepared with an analogous procedure to that described in Step 1; Scheme 10, and by reacting the precursor (5) with suitable reagents.

A diastereomeric mixture was obtained from (5) which was were separated by means of preparative HPLC instrument (Method 1 General Experimental Details section) to give the two diastereomers, (16) and (17) identified as fast and slow isomer, respectively, according to their observed retention times under the chromatographic conditions described in the General Experimental Details section (Method 1).

TABLE 3 HPLC-MS characterization t_(R)/min Dia- MS/ Me- stereo- Pre- En- SALT ESI⁺ thods meric cur- try Structure NAME [MH]⁺ 1 or 2 ratio ¹H NMR [α]_(D) sor 16

Free Base 696.0 6.52 (1) >99:1 ¹H NMR (400 MHz, DMSO- d₆) δ ppm 8.55 (s, 2 H), 7.32-7.43 (m, 4 H), 7.17 (m, 1 H), 7.05-7.11 (m, 2 H), 6.92-6.97 (m, 1 H), 5.83- 5.96 (m, 1 H), 4.74 (s, 1 H), 3.90 (d, J = 7.06 Hz, 2 H), 3.56 (d, J = 8.38 Hz, 2 H), 3.36 (m, 4 H), 3.07-3.26 (m, 2 H), 2.84 and 3.04 (2s, 6 H), 1.16-1.30 (m, 1 H), 0.58 (m, 2 H), 0.34 (d, J = 3.97 Hz, 2 H). 5 17

Free Base 695.9 6.87 (1) >99:1 ¹H NMR (400 MHz δ ppm 8.56-8.67 (m, 2 H), 7.29-7.37 (m, 4 H), 7.20 (d, J = 7.94 Hz, 1 H), 7.05-7.11 (m, 2 H), 6.88- 6.95 (m, 1 H), 5.88 (dd, J = 10.14, 4.41 Hz, 1H), 4.85 (s, 1 H), 3.76-3.96 (m, 2 H), 3.50-3.69 (m, 2 H), 3.07-3.46 (m, 6 H), 2.83 and 3.02 (2s, 6 H), 1.18-1.30 (m, 1 H), 0.47-0.66 (m, 2 H), 0.22-0.42 (m, 2 H). 5

Example 3 Synthesis of 3,5-dichloro-4-((S)-2-((S)-1-(4-(cyclopropylmethoxy)-3-(methylsulfonamido)benzoyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide (19)

Step 1: 4-((S)-2-((S)-1-(3-(N-(tert-butoxycarbonyl)methylsulfonamido)-4-(cyclopropylmethoxy)benzoyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (18)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (3) (40 mg; 0.077 mmol) was placed in a 50 ml round bottom flask and dissolved in DMF (2 ml). 3-(N-(tert-butoxycarbonyl)methylsulfonamido)-4-(cyclopropylmethoxy)benzoic acid (40 mg, 0.104 mmol, obtainable as described in WO 2010/089107, which is incorporated herein by reference in its entirety), was added to the reaction solution followed by EDC (20.0 mg, 0.104 mmol) and DMAP (15.0 mg, 0.123 mmol). The reaction was stirred at RT for 6 hours to get to completion and quenched by adding 20 ml of aq HCl 1M. The aqueous layer was extracted with EtOAc and washed with HCl 1M (×3) and with aq K₂CO₃ 5% (×3). The resulting organic extract was dried with Na₂SO₄, filtered on a filter paper, and the solvent removed on a rotary evaporator under reduced pressure. The oil residue was purified by preparative HPLC (Method 1) to yield 30 mg of desired product (yield 44%).

MS/ESI⁺ 884.1 [MH]⁺

¹H NMR (400 MHz, acetone) δ ppm 8.28 (s, 2H), 7.33 (d, J=7.94 Hz, 1H), 7.14-7.23 (m, 4H), 6.68-7.13 (m, 2H), 6.16 (dd, J=9.92, 4.19 Hz, 1H), 4.52 (dd, J=7.94, 6.17 Hz, 1H), 3.88-4.12 (m, 6H), 3.56-3.74 (m, 3H), 3.53 (s, 3H), 3.34 (dd, J=14.11, 4.41 Hz, 1H), 1.74-1.93 (m, 2H), 1.47 (s, 9H), 1.25-1.35 (m, 2H), 0.51-0.69 (m, 4H), 0.27-0.48 (m, 4H).

Step 2: 3,5-dichloro-4-((S)-2-((S)-1-(4-(cyclopropylmethoxy)-3-(methylsulfonamido)benzoyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide (19)

4-((S)-2-((S)-1-(3-(N-(tert-butoxycarbonyl)methylsulfonamido)-4-(cyclopropylmethoxy)benzo yl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (18) (30 mg, 0.034 mmol) was dissolved in HCl/EOAc (4M; 2 ml) and stirred for 10 hours at RT to achieve completion. The reaction was quenched by adding K₂CO₃ 5% and extracted with EtOAc. The resulting organic extract was dried over Na₂SO₄, filtered on a filter paper, and the solvent removed on a rotary evaporator under reduced pressure. The residue was recrystallised from EtOH:hexane (1:3) to yield a white solid (18 mg; yield 68%) of the title compound. MS/ESI⁺ 784.1 [MH]⁺; t_(R)=5.72 (Method 1); [α_(D)]=−48.92 (c=3.7; DCM); Diastereomeric Ratio >99:1.

¹H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.16 (br. s., 2H), 7.53 (m, 1H), 7.09-7.20 (m, 3H), 7.05 (m, 1H), 6.96 (m, 2H), 6.41-6.63-6.84 (t, 1H, CHF₂), 6.08-6.17 (m, 1H), 4.53-4.66 (m, 1H), 3.81-3.98 (m, 4H), 3.61 (m, 3H), 3.22-3.39 (m, 1H), 3.02 (s, 3H), 2.20-2.34 (m, 1H), 1.78-2.02 (m, 3H), 1.27 (m, 2H), 0.59-0.75 (m, 4H), 0.28-0.42 (m, 4H).

The compounds listed in Table 4 were prepared with an analogous procedure to that described above in Example 3, Scheme 11, by reacting the appropriate precursors listed with suitable reagents, followed by a purification step as indicated in the table below in place of recrystallization above described.

TABLE 4 HPLC-MS characterization t_(R)/min Puri- MS/ Me- Diastereo- Pre- fica- En- SALT ESI⁺ thods meric cur- tion try Structure NAME [MH]⁺ 1 or 2 ratio ¹H NMR sor method 20

formate 669.3 3.07 (2) 99:1  5 Pre- para- tive HPLC 21

hydro- chloride 668.3 2.57 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 9.54 (bs, 1 H), 8.57 (s, 2 H), 7.40-7.65 (m, 4 H), 7.20 (d, J = 7.94 Hz, 1 H), 7.10 (m, 2 H), 6.95-7.04 (m, 1 H), 5.91-6.13 (m, 1 H), 5.51 (s, 1 H), 4.04-4.21 (m, 3 H), 3.83-4.03 (m, 2 H), 3.67-3.82 (m, 1 H), 3.25-3.37 (m, 2 H), 3.19 (m, 4 H), 1.09-1.32 (m, 1 H), 0.56 (d, J = 7.94 Hz, 2 H), 0.32 (d, J = 4.41 Hz, 2 H) 6 Filtra- tion of the hydro- chloride salt from reac- tion mix- ture 22

formate 682.3 2.69; 2.82 (2) 14:86 5 Pre- para- tive HPLC

Example 4 Synthesis of 4-((2S)-2-(3-(4-aminobenzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (26)

Step 1: methyl 3-(4-nitrobenzoyl)thiazolidine-2-carboxylate (23)

Methyl thiazolidine-2-carboxylate hydrochloride (200 mg, 1.089 mmol) was dissolved in DCM (2 ml). DMAP (173 mg, 1.416 mmol) and 4-nitrobenzoyl chloride (263 mg, 1.416 mmol) were added, and the reaction was stirred at RT for 2 hours to achieve completion. The reaction mixture was diluted with DMC and extracted with aq HCl 1M. The organic phase was washed with HCl 1N and brine, dried over Na₂SO₄ and concentrated under vacuum to give methyl 3-(4-nitrobenzoyl)thiazolidine-2-carboxylate (220 mg, 0.742 mmol, 68% yield). MS/ESI⁺ 297.05 [MH]⁺

Step 2: 3-(4-nitrobenzoyl)thiazolidine-2-carboxylic acid (24)

Methyl 3-(4-nitrobenzoyl)thiazolidine-2-carboxylate (220 mg, 0.742 mmol) was dissolved in THF (2 ml). LiOH 1M (1 ml, 1.000 mmol) was added, and the reaction was stirred at RT for 6 hours to achieve completion. The reaction mixture was diluted with HCl 1N and extracted with EtOAc. The organic phase was dried over Na₂SO₄ and concentrated under vacuum to give 3-(4-nitrobenzoyl)thiazolidine-2-carboxylic acid (180 mg, 0.638 mmol, 86% yield). MS/ESI⁺ 283.03 [MH]⁺

Step 3: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-nitrobenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (25)

(S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (100 mg, 0.238 mmol), 3-(4-nitrobenzoyl)thiazolidine-2-carboxylic acid (134 mg, 0.476 mmol), DMAP (34.9 mg, 0.286 mmol), and EDC (137 mg, 0.714 mmol) were dissolved in DMF (1.5 ml). The reaction was stirred at RT for 2 hours to achieve completion. The reaction mixture was diluted with water, and the precipitate was washed with water, dissolved in EtOAc and extracted with HCl 1N, Na₂CO₃ sat. sol. and brine. The organic phase was dried over Na₂SO₄ and concentrated under vacuum to give 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-nitrobenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (130 mg, 0.190 mmol, 80% yield).

MS/ESI⁺ 684.07 [MH]⁺

Step 4: 4-((2S)-2-(3-(4-aminobenzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (26) 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-nitrobenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (130 mg, 0.190 mmol) was dissolved in THF (3 ml). Tin(II) chloride dihydrate (257 mg, 1.140 mmol) was added, and the mixture was stirred at RT for 4 days. The solvent was removed under vacuum, and the crude product was dissolved in EtOAc and diluted with Na₂CO₃ sat. sol. Diatomaceus earth was added to the two phases, and the mixture was filtered on a Diatomaceus earth pad. The organic phase was washed with Na₂CO₃ sat. sol., brine, dried over Na₂SO₄ and concentrated under vacuum. The crude product was triturated in Et₂O to give 4-((2S)-2-(3-(4-aminobenzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyeethyl)-3,5-dichloropyridine 1-oxide (30 mg, 0.046 mmol, 24% yield). MS/ESI⁺ 653.8 [MH]⁺; t_(R)=5.80; 6.00 (Method 1); Diastereomeric Ratio 30:70. Example 5 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(4-methoxy-3-(methylsulfonyloxy)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-(30)

Step 1: 5-formyl-2-methoxyphenyl methanesulfonate (28)

3-hydroxy-4-methoxybenzaldehyde (27) (0.5 g, 3.291 mmol) was dissolved in DCM, and methanesulfonyl chloride (0.376 g, 3.29 mmol) followed by triethylamine (0.499 g, 4.931 mmol) were added. The reaction solution was stirred at RT for 2 hours, after that time, it was quenched with aq HCl 1M and extracted with EtOAc. The organic extract was then washed with aq K₂CO₃ 5%, dried over Na₂SO₄ and the solvent removed on a rotary evaporator. The desired product was obtained as a white powder (0.750 g, yield 99%). MS/ESI⁺ 231.02 [MH]⁺

Step 2: 4-methoxy-3-(methylsulfonyloxy)benzoic acid (29)

5-formyl-2-methoxyphenyl methanesulfonate (28) (0.750 g, 3.261 mmol) and sulfamic acid (0.316 g, 3.261 mmol) were dissolved in acetic acid (10 ml) and cooled down by ice bath. Sodium chlorite (0.589 g, 6.521 mmol) was dissolved in water (4 ml) and slowly added to the cold reaction solution. The reaction mixture was allowed to warm at RT and stirred for about 2 hours. After that time, full conversion was observed by UPLC-MS analysis. Addition of water (15 ml) caused precipitation of a white solid, which was filtered and washed several times with water (0.700 g, yield 87%).

MS/ESI⁺ 247.02 [MH]⁺

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro methoxy)phenyl)-2-((S)-1-(4-methoxy-3-(methylsulfonyloxy)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (30)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(4-methoxy-3-(methylsulfonyloxy)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine-1-oxide (30) was prepared by following an analogous procedure to that described in Step 1 (Example 3). MS/ESI⁺ 745.0 [MH]⁺; [α_(D)]=31.30 (c=0.34; CHCl₃), t_(R)=5.57 (Method 1); Diastereomeric Ratio >99:1. ¹H NMR (400 MHz, CHLOROFORM-d) δ ppm 8.17 (s, 2H), 7.56 (m, 2H), 7.13 (m, 4H), 6.60 (t, J=75.00 Hz, 1H), 6.04-6.21 (m, 1H), 4.46-4.75 (m, 1H), 3.95 (s, 3H), 3.85 (m, 2H), 3.50-3.70 (m, 3H), 3.25-3.31 (m, 1H), 3.22 (s, 3H), 2.19-2.41 (m, 1H), 1.74-2.03 (m, 3H), 1.14-1.34 (m, 1H), 0.64 (d, J=7.09 Hz, 2H), 0.34 (d, J=4.16 Hz, 2H).

The compounds listed in Table 5 were prepared according to an analogous procedure to that described in Step 3 (Scheme 13) and by reacting the appropriate precursors listed with suitable commercial reagents, followed by an appropriate purification step in place of preparative HPLC as below indicated.

TABLE 5 HPLC-MS characterization t_(R)/min Purification Entry Structure SALT NAME MS/ES⁺ [MH]⁺ Methods 1 or 2 Distereomeric ratio ¹H NMR Precursor Method 31

Free Base 768.65 2.65; 2.82 (2) 6:94 ¹H NMR (400 MHz, DMSO- d₆) δ ppm 8.56 (s, 1 H), 7.36- 7.55 (m, 2 H), 7.16-7.21 (m, 1 H), 7.01-7.11 (m, 3 H), 6.92- 6.99 (m, 1 H), 5.93-6.05 (m, 1 H), 5.52 (s, 1 H), 3.92-4.12 (m, 1 H), 3.84 (m, 6 H), 3.52- 3.64 (m, 4 H), 3.47 (m, 3 H), 3.25-3.29 (m, 1 H), 3.06-3.18 (m, 1 H), 2.89-3.03 (m, 1 H), 2.38 (m, 4 H) 1.09-1.20 (m, 1 H), 0.46-.61 (m, 2 H), 0.19- 0.29 (m, 2 H). 5 Filtration of the precipitation obtained after water addition, and trituration with MeOH 32

Free Base 776.65 3.77; 3.81 (2) 38:62 5 Preparative HPLC 33

Free Base 738.62 2.56; 2.69 (2) 38:62 5 Preparative HPLC 34

Free Base 696.3 2.49; 2.67 (2) 16:84 5 Preparative HPLC 35

Free Base 630.2 3.19; 3.29 (2) 24:76 5 No purification of the crude performed 36

Free Base 772.2 4.14 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.36-7.45 (m, 2 H), 7.15-7.22 (m, 1 H), 7.01-7.12 (m, 4 H), 6.92-7.00 (m, 1 H), 5.94-6.06 (m, 1 H), 5.50 (s, 1 H), 3.97-4.11 (m, 1 H), 3.84 (m, 7 H), 3.39-3.50 (m, 1 H), 3.26(d, J = 5.73 Hz, 1 H), 3.12 (m, 5 H), 2.91-3.04 (m, 1 H), 1.12-1.30 (m, 1 H), 0.45-0.61 (m, 2 H), 0.24-0.32 (m, 2 H). 6 Tituration with MeOH 37

Free Base 682.2 3.75 (2) 96:4 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.47-8.73 (m, 2 H), 8.07-8.20 (m, 1 H), 7.91-8.04 (m, 2 H), 7.49-7.65 (m, 2 H), 7.16-7.22 (m, 1 H), 7.07-7.14 (m, 1 H), 6.93-7.03 (m, 1 H), 5.86-6.12 (m, 1 H), 5.53 (s, 1 H), 3.68-4.00 (m, 5 H), 3.39- 3.54 (m, 1 H), 3.06-3.21 (m, 1 H), 2.89-3.05 (m, 1 H), 1.06- 1.32 (m, 1 H), 0.42-0.64 (m, 2 H), 0.12-0.36 (m, 2 H). 6 Trituration with MeOH 38

Free Base 646.2 3.32; 3.40 (2) 11:89 5 Trituration with MeOH 39

formate 738.3 2.67 (2) 98:2 ¹H NMR (400 MHz, DMSO- d6) δ ppm 8.56 (s, 2 H), 7.31- 7.52 (m, 4 H), 7.14-7.22 (m, 1 H), 7.05-7.12 (m, 2 H), 6.93- 7.00 (m, 1 H), 5.93-6.14 (m, 1 H), 5.50 (s, 1 H), 3.89-3.97 (m, 1 H), 3.82-3.88 (m, 2 H), 3.70-3.81 (m, 1 H), 3.58 (m, 4 H), 3.52 (s, 2 H), 3.41-3.48 (m, 1 H), 3.20-3.25 (m, 1 H), 3.06-3.18 (m, 1 H), 2.93-3.03 (m, 1 H), 2.28-2.41 (m, 4 H), 1.13-1.21 (m, 1 H), 0.45-0.64 (m, 2 H), 0.19-0.33 (m, 2 H) 6 No purification of the crude performed 40

Free Base 786.2 3.58 (2) 97:3 ¹H NMR (400 MHz, DMSO- d6) δ ppm 8.56 (s, 2 H), 7.33- 7.50 (m, 4 H), 7.15-7.22 (m, 1 H), 7.06-7.12 (m, 2 H), 6.93- 7.00 (m, 1 H), 5.93-6.10 (m, 1 H), 5.50 (s, 1 H), 3.90-4.00 (m, 1 H), 3.83-3.88 (m, 2 H), 3.73 (m, 3 H), 3.37-3.52 (m, 2 H), 3.05-3.21 (m, 5 H), 2.94- 3.04 (m, 1 H), 2.82-2.92 (m, 4 H), 1.11-1.28 (m, 1 H), 0.46- 0.61 (m, 2 H), 0.17-0.41 (m, 2 H). 6 Trituration with EtOH 41

Free Base 706.2 3.73 (2) >99:1 ¹H NMR (400 MHz, DMSO- d6) δ ppm 8.53-8.64 (s, 1 H), 8.43-8.51 (s, 2 H), 7.73-7.93 (m, 3 H), 7.37-7.67 (m, 2 H), 7.14-7.22 (m, 1 H), 7.05-7.13 (m, 2 H), 6.96-7.04 (m, 1 H), 5.98-6.12 (m, 1 H), 5.53 (s, 1 H), 3.74-3.99 (m, 4 H), 3.41- 3.57 (m, 1 H), 3.07-3.20 (m, 2 H), 2.92-3.06 (m, 1 H), 1.06- 1.29 (m, 1 H), 0.47-0.62 (m, 2 H), 0.13-0.37 (m, 2 H) 6 No purification of the crude performed 42

formate 640.3 4.05; 4.15 (2) 38:62 5 Preparative HPLC 184

Free Base 621.3 80:20 (¹H NMR) 185

Free Base 692.2 3.14 (2) 98/2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.47-7.65 (m, 4 H), 7.11-7.25 (m, 2 H), 7.07 (t, J = 75.00 Hz, 1 H), 7.04 (d, J = 1.76 Hz, 1 H), 5.98-6.10 (m, 1 H), 4.49 (s, 1 H), 3.89- 4.02 (m, 2 H), 3.34-3.64 (m, 4 H), 2.82-3.03 (m, 6 H), 2.14- 2.29 (m, 1 H), 1.85 (t, J = 6.62 Hz, 2 H), 1.55-1.67 (m, 1 H), 1.12-1.30 (m, 1 H), 0.54 (dd, J = 8.16, 1.54 Hz, 3 H), 0.30 (d, J = 4.41 Hz, 2 H). 186

Free Base 639.1 3.92 >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.34-7.59 (m, 5 H), 7.13-7.21 (m, 1 H), 7.08 (s, 2 H), 6.93-7.01 (m, 1 H), 5.93-6.11 (m, 1 H), 5.40- 5.59 (m, 1 H), 3.83-4.03 (m, 3 H), 3.69-3.82 (m, 1 H), 3.40- 3.54 (m, 1 H), 3.05-3.18 (m, 1 H), 2.93-3.04 (m, 1 H), 1.14- 1.28 (m, 1 H), 0.46-0.63 (m, 2 H), 0.22-0.40 (m, 2 H). 187

Free Base 710.2 3.38 (2) 3/97 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.40-7.65 (m, 4 H), 6.78-7.31 (m, 4 H), 5.85-6.14 (m, 1 H), 5.24 (s, 1 H), 3.69-4.02 (m, 4 H), 3.36- 3.63 (m, 2 H), 3.09-3.21 (m, 1 H), 2.74-3.07 (m, 7 H), 1.12- 1.28 (m, 1 H), 0.42-0.66 (m, 2 H), 0.18-0.39 (m, 2 H)

The compounds listed in Table 14 were prepared according to an analogous procedure to that described in Step 3 (Scheme 13) and by reacting the appropriate precursors listed with suitable commercial reagents using DCM instead of DMF as the solvent, followed by an appropriate purification step as below indicated. Compounds 193, 194, and 195 were prepared starting from intermediate 3 or 179 obtained as free bases after a basic treatment of hydrochloride salts with aqueous 1M NaHCO₃ followed by extraction with DCM.

TABLE 14 HPLC-MS characterization t_(R)/min Diastereo- MS/ESI⁺ Method meric Purification Entry Structure SALT NAME [MH]⁺ 1, 2 or 3 ratio ¹H NMR [α] _(D) Precursor Method 188

Free Base 653.24 4.03 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆ 353K) δ ppm 8.38 (s, 2 H), 7.18-7.36 (m, 5 H), 7.15 (d, 1 H), 7.08 (d, 1 H), 6.94 (dd, 1 H), 6.98 (t, 1 H), 6.01 (dd, 1 H), 5.50 (br. s., 1 H), 3.95-4.10 (m, 1 H), 3.92 (d, 2 H), 3.63- 3.89 (m, 3 H), 3.47 (dd, 1 H), 3.31 (dd, 1 H), 3.06-3.23 (m, 2 H), 1.06-1.37 (m, 1 H), 0.47-0.69 (m, 2 H), 0.21-0.46 (m, 2 H) −33.6 (c = 0.46, DCM) 6 Treatment with polymer supported isocyanate scavenger followed by preparative HPLC (Method 2) 189

Free Base 617.08 3.78 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.16 (d, 1 H), 7.04-7.10 (m, 1 H), 6.93 (dd, 1 H), 7.07 (t, 1 H), 5.95 (dd, 1 H), 5.37 and 5.64 (s, 1 H), 3.93 (d, 2 H), 3.84 (dd, 2 H), 3.42 (dd, 1 H), 3.28 (dd, 1 H), 3.16 (dt, 1 H), 2.93-3.07 (m, 1 H), 2.32 (d, 2 H), 1.10-1.36 (m, 1 H), 0.84- 1.04 (m, 1 H), 0.51-0.67 (m, 2 H), 0.40-0.51 (m, 2 H), 0.26-0.39 (m, 2 H), −0.03-0.18 (m, 2 H) −42.5 (c = 0.54, DCM) 6 Preparative HPLC (Method 2) 190

Free Base 731.3 3.85 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.52 (s, 2 H), 7.87-8.01 (m, 2 H), 7.73- 7.84 (m, 1 H), 7.58-7.73 (m, 2 H), 7.16 (d, 1 H), 7.05 (d, 1 H), 6.92 (dd, 1 H), 7.07 (t, 1 H), 5.93 (dd, 1 H), 5.17 (s, 1 H), 3.91 (d, 2 H), 3.70-3.88 (m, 2 H), 3.35-3.63 (m, 4 H), 2.76-3.25 (m, 4 H), 1.08-1.31 (m, 1 H), 0.43-0.69 (m, 2 H), 0.20-0.43 (m, 2 H) −27.4 (c = 0.3, DCM) 6 Flash chromato- graphy on silca gel followed by preparative HPLC (Method 3) 191

trifluoroacetate 676.01 3.19 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 9.41 (br. s., 1 H), 8.56 (s, 2 H), 7.22 (d, 1 H), 7.10 (d, 1 H), 6.98 (dd, 1 H), 7.09 (t, 1 H), 6.04 (dd, 1 H), 5.29 (s, 1 H), 3.96-4.15 (m, 2 H), 3.93 (d, 2 H), 3.62-3.90 (m, 4 H), 3.00-3.37 (m, 10 H), 2.90 (t, 2 H), 1.07- 1.45 (m, 1 H), 0.51-0.68 (m, 2 H), 0.28- 0.44 (m, 2 H) −27.1 (c = 0.5, DCM) 6 Preparative HPLC (Method 3) 192

trifluoroacetate mono salt 689.44 2.92 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.20 (d, 1 H), 7.08 (s, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.00 (dd, 1 H), 5.30 (s, 1 H), 3.93 (d, 2 H), 2.75-3.84 (m, 18 H), 2.76 (s, 3 H), 1.11-1.40 (m, 1 H), 0.49-0.66 (m, 2 H), 0.24-0.44 (m, 2 H) −32.4 (c = 0.3, DCM) 6 Preparative HPLC (Method 3) 193

Free Base 692.43 3.39 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆ 353K) δ ppm 8.41 (s, 2 H), 7.37-7.61 (m, 4 H), 7.15 (d, 1 H), 7.07 (d, 1 H), 6.96 (dd, 1 H), 6.97 (t, 1 H), 6.01 (br. s., 1 H), 4.52 (dd, 1 H), 3.88 (d, 2 H), 3.50-3.64 (m, 2 H), 3.15-3.29 (m, 2 H), 2.97 (s, 6 H), 2.16-2.42 (m, 1 H), 1.52-2.03 (m, 3 H), 0.99-1.32 (m, 1 H), 0.42-0.73 (m, 2 H), 0.14-0.40 (m, 2 H) −32.8 (c = 0.51, DCM) Free base of 3 Preparative HPLC (Method 2) 194

Free Base 635.34 3.88 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.36-7.52 (m, 5 H), 7.19 (d, 1 H), 7.12 (br. s., 1 H), 6.99 (d, 1 H), 7.07 (t, 1 H), 5.87-6.14 (m, 1 H), 4.28 (br. s., 1 H), 3.91 (d, 2 H), 3.32-3.56 (m, 2 H), 3.13-3.32 (m, 2 H), 2.95 (dd, 1 H), 2.39-2.46 (m, 1 H), 1.91-2.10 (m, 1 H), 1.59-1.90 (m, 2 H), 1.35-1.59 (m, 1 H), 1.08-1.33 (m, 1 H), 0.45-0.71 (m, 2 H), 0.08-0.45 (m, 2 H) −60.9 (c = 0.72, DCM) Free Base of 179 Preparative HPLC (Method 2) 195

Free Base 706.38 3.42 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.41-7.55 (m, 4 H), 7.18 (d, 1 H), 7.12 (s, 1 H), 6.99 (d, 1 H), 7.07 (t, 1 H), 6.00 (dd, 1 H), 4.18-4.45 (m, 1 H), 3.91 (d, 2 H), 3.77-4.01 (m, 2 H), 3.34-3.58 (m, 2 H), 3.15-3.34 (m, 2 H), 2.98 (br. s., 3 H), 2.91 (br. s., 3 H), 1.90-2.13 (m, 1 H), 1.60-1.90 (m, 2 H), 1.34-1.60 (m, 1 H), 1.02-1.32 (m, 1 H), 0.49-0.67 (m, 2 H), 0.24-0.42 (m, 2 H) −60.1 (c = 0.48, DCM) Free base of 179 Preparative HPLC (Method 2)

Example 20 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)acetyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (198)

Step 1: 3-((1,3-dioxolan-2-yl)methyl)-N,N-dimethylbenzamide (196) 3-((1,3-dioxolan-2-yl)methyl)benzoic acid (250 mg, 1.201 mmol), dimethylamine hydrochloride (147 mg, 1.801 mmol), EDC (345 mg, 1.801 mmol), and DMAP (513 mg, 4.20 mmol) were dissolved in DCM (30 ml) and the solution was stirred at RT for 1 hour. The reaction mixture was washed twice with 1N HCl, and the organic layer was dried over Na₂SO₄. The solvent was removed under reduced pressure to give the desired product (244 mg, 1.037 mmol, 86% yield) MS/ESI⁺ 236.18 [MH]⁺ Step 2: 2-(3-(dimethylcarbamoyl)phenyl)acetic acid (197)

To a solution of 3-((1,3-dioxolan-2-yl)methyl)-N,N-dimethylbenzamide (244 mg, 1.037 mmol) in THF (30 ml), water (20 ml), oxone (1913 mg, 3.11 mmol), and aqueous 37% HCl (2 ml, 23.92 mmol) were added, and the mixture was stirred at RT for 24 hours. Additional oxone (1.0 g, 1.627 mmol) and aqueous 37% HCl (1 ml, 11.96 mmol) were added, and the stirring was continued at RT for further 24 hours. The reaction mixture was diluted with water (100 ml) and extracted twice with DCM; (2×70 ml); the combined organic layers were dried over Na₂SO₄ and evaporated to dryness to afford the desired product (200 mg, 0.965 mmol, 93% yield) MS/ESI⁺ 208.20 [MH]⁺.

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)acetyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (198)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)acetyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide was prepared according to an analogous procedure to that described in Step 3 (Scheme 13) Example 5, using DCM as the solvent. It was purified by treatment with polymer supported isocyanate followed by preparative HPLC (Method 2) (10% yield).

MS/ESI⁺ 724.28 [MH]⁺, t_(R)=3.82 min (Method 3); Diastereomeric Ratio >95:5 (¹H NMR);

¹H NMR (300 MHz, DMSO-d6) δ ppm 8.52 (s, 2H), 7.23-7.48 (m, 4H), 7.15 (d, 1H), 7.06 (d, 1H), 6.91 (dd, 1H), 6.79-7.43 (m, 1H), 5.93 (dd, 1H), 5.41 (s, 1H), 3.93 (dd, 2H), 3.88 (d, 2H), 3.82 (s, 2H), 3.41 (dd, 1H), 3.27 (dd, 1H), 3.00-3.22 (m, 2H), 2.96 (br. s., 3H), 2.90 (br. s., 3H), 1.06-1.39 (m, 1H), 0.46-0.63 (m, 2H), 0.06-0.41 (m, 2H)

The compound listed in Table 15 was prepared according to an analogous procedure to that described in Scheme 27 and by reacting the appropriate precursor listed (obtained as free base after basic treatment of hydrochloride salt with aqueous sat. NaHCO₃ followed by extraction with DCM), followed by an appropriate purification step as below indicated.

TABLE 15 HPLC-MS characterization SALT MS/ESI⁺ t_(R)/min Method Diastereomeric Entry Structure NAME [MH]⁺ 1, 2 or 3 ratio 199

Free Base 706.36 3.50 (3) >95:5 (¹H NMR B) Pur- Pre- ification Entry ¹H NMR [α] _(D) cursor Method 199 ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.56 (s, 2 H), 7.23-7.43 (m, 4 H), 7.13 (d, 1 H), 7.06 (d, 1 H), 6.90 (dd, 1 H), 7.05 (t, 1 H), 5.88 (dd, 1 H), 4.32 (dd, 1 H), 3.78-3.95 (m, 2 H), 3.73 (s, 2 H), 3.49-3.67 (m, 2 H), 3.39 (dd, 1 H), 3.22 (dd, 1 H), 2.94 (br. s., 3 H), 2.90 (br. s., 3 H), 2.05-2.24 (m, 1 H), 1.76-1.95 (m, 1 H), 1.47-1.76 (m, 2 H), 1.05-1.23 (m, 1 H), 0.46-0.62 (m, 2 H), 0.20-0.38 (m, 2 H) −18.2 (c = 0.57, DCM). Free base of 3 Preparative HPLC (Method 2) folowed by flash chromato- graphy on silica gel

Example 6 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide formate (49)

Step 1: methyl 3-(cyclopropylmethoxy)-5-nitrobenzoate (44)

Methyl 3-hydroxy-5-nitrobenzoate (43) (1.6 g, 8.1 mmol) was dissolved in DMF (15 ml). (Bromomethyl)cyclopropane (2.2 g, 16.2 mmol) and K₂CO₃ (1.7 g, 12.2 mmol) were added, and the mixture was stirred at 80° C. for 2 hours. The reaction was cooled at RT, diluted with water and filtered. The precipitate was dissolved in ethyl acetate, and the organic phase was dried over Na₂SO₄ and evaporated under vacuum to give 1.65 g of the desired product (yield 81%).

MS/ESI⁺ 252.08 [MH]⁺

Step 2: methyl 3-amino-5-(cyclopropylmethoxy)benzoate (45)

Methyl 3-(cyclopropylmethoxy)-5-nitrobenzoate (44) (4.9 g, 19.5 mmol) was dissolved in MeOH (200 ml), and Pd/C₅% (1.5 g, 0.7 mmol) was added. The solution was shaken under hydrogen atmosphere on a Parr apparatus at 40 psi for 1 hour. The catalyst was filtered on a Diatomaceus earth pad, and the solvent was evaporated under vacuum to give 3.67 g of the desired product (yield 85%).

MS/ESI⁺ 222.11 [MH]⁺

Step 3: methyl 3-(cyclopropylmethoxy)-5-(methylsulfonamido)benzoate (46)

Methyl 3-amino-5-(cyclopropylmethoxy)benzoate (45) (1.3 g, 5.9 mmol) was dissolved in pyridine (4 ml). Methanesulfonyl chloride (0.6 ml, 7.7 mmol) was added slowly at 0° C., and the mixture was stirred at RT for 2.5 hours. The reaction was diluted with aq HCl 1N, and the product was extracted with ethyl acetate. The organic phase was washed with HCl 1N, dried over Na₂SO₄ and evaporated under vacuum to give 1.7 g of the desired product (yield 97%). MS/ESI⁺ 300.08 [MH]⁺

Step 4: methyl 3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoate (47)

Methyl 3-(cyclopropylmethoxy)-5-(methylsulfonamido)benzoate (46) (3 g, 10.02 mmol) was dissolved in DMF (25 ml). 4-(2-chloroethyl)morpholine (4.5 g, 30.1 mmol) and K₂CO₃ (2.1 g, 15.03 mmol) were added, and the mixture was stirred at 60° C. for 2 hours. The reaction was diluted with water and extracted with ethyl acetate. The organic phase was washed with water, dried over Na₂SO₄ and evaporated under vacuum to give 3 g of the desired product (yield 73%).

MS/ESI⁺ 413.17 [MH]⁺

Step 5: 3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoic acid (48)

Methyl 3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoate (47) (3 g, 7.3 mmol) was dissolved in MeOH (45 ml). Aq. NaOH 1N (9 ml) was added, and the mixture was stirred at RT overnight. The reaction was diluted with aq. HCl 1N (9 ml), and the solvent was removed under vacuum to yield 3.7 g of the desired product (quantitative yield).

MS/ESI⁺ 399.15 [MH]⁺

Step 6: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide formate (49)

Compound (49) was prepared according to an analogous procedure to that described in Example 3, step 1, starting from compound 5. The crude product was purified by preparative HPLC to obtain compound (49) as a formate salt.

MS/ESI⁺ 915.3 [MH]⁺; t_(R)=3.37; 3.43 (Method 2); Diastereomeric Ratio=47:53.

Example 7 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-((dimethylamino)methyl)thiophene-2-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide formate (51)

Step 1: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-formylthiophene-2-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (50) 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (5) (200 mg, 0.374 mmol), 5-formylthiophene-2-carboxylic acid (233 mg, 1.494 mmol), DMAP (100 mg, 0.822 mmol), and EDC (358 mg, 1.868 mmol) were dissolved in DMF (2 ml). The reaction was stirred at RT overnight, then it was diluted with water, and the precipitate was washed with water, dissolved in AcOEt and washed with aq. HCl 1N, aq. Na₂CO₃ sat. sol., and brine. The organic phase was dried over Na₂SO₄ and concentrated under vacuum to give 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-formylthiophene-2-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (150 mg, yield 60%).

MS/ESI⁺ 673.04 [MH]⁺

Step 2: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-((dimethylamino)methyl)thiophene-2-carbonyl)thiazolidine-2-carbonyl oxy)ethyl)pyridine 1-oxide (51)

3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-formyl benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (50) (50 mg, 0.075 mmol) was dissolved in THF (1 ml). Acetic acid (8.58 μl, 0.150 mmol) and dimethylamine 2M in THF (7.95 μl, 0.150 mmol) were added, and the mixture was stirred at RT for 30 minutes. Sodium triacetoxyborohydride (32 mg, 0.150 mmol) was added, and the mixture was stirred at RT for 3 hours to achieve completion. The reaction mixture was diluted with water and extracted with AcOEt. The organic phase was dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by semi-preparative HPLC (Method 1) to give the wanted product as formate salt (16 mg, yield 31%). MS/ESI⁺ 702.2 [MH]⁺; t_(R) (Method 2)=2.54; 2.68 min; Diastereomeric Ratio=21:79

Example 8 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (52)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (300 mg, 0.525 mmol) was dissolved in Py (3 ml, 37.1 mmol). 3-(dimethylcarbamoyl)benzene-1-sulfonyl chloride (156 mg, 0.630 mmol) was added, and the reaction was stirred at RT for 4 hours to achieve completion. The reaction mixture was diluted with aqueous HCl 1N, and extracted with ethyl acetate. The organic phase was washed with aqueous HCl 1N and brine, dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by flash chromatography (DCM/IsoPrOH 98/2) to give 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (250 mg, 0.335 mmol, 63.8% yield).

MS/ESI⁺ 746.2 [MH]⁺; [α]_(D)]=−43.30 (c=0.51; CHCl₃), t_(R)=3.66 (Method 1); Diastereomeric Ratio=>99/1; ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2H), 7.88-7.97 (m, 1H), 7.75-7.82 (m, 1H), 7.68-7.74 (m, 1H), 7.14-7.21 (m, 1H), 7.09-7.13 (m, 1H), 7.08 (t, J=75.00 Hz, 1H), 6.92-6.99 (m, 1H), 5.91-6.10 (m, 1H), 5.54 (s, 1 H), 3.79-3.94 (m, 3H), 3.60-3.71 (m, 1H), 3.41-3.51 (m, 1H), 3.26-3.32 (m, 1H),3.02 (s, 3H), 2.92-3.00 (m, 1H), 2.89 (s, 3H), 2.56-2.70 (m, 1H), 1.20-1.27 (m, 1H), 0.53-0.60 (m, 1H), 0.29-0.36 (m, 1H).

The compounds listed in Table 6 were prepared according to an analogous procedure to that described for Scheme 16 by reacting the appropriate precursors listed with commercial suitable reagents, followed by appropriate purification step as below reported, if needed. Heating under MW irradiation (50° C., 30 minutes) was used for the synthesis of compound 224.

TABLE 6 HPLC-MS characterization MS/ t_(R)/min Diaste- SALT ESI⁺ Method reomeric Purification Entry Structure NAME [MH]⁺ 1, 2 or 3 ratio ¹H NMR [α] _(D) Precursor Method 53

Free Base 717.2  6.97 (1) >99:1 1H NMR (400 MHz, acetone) δ ppm 8.30 (s, 2 H), 7.39-7.48 (m, 1 H), 7.25-7.35 (m, 2 H), 7.17 (dd, J = 14.77, 8.16 Hz, 2 H), 7.03- 7.10 (m, 1 H), 6.93 (t, J = 75.00 Hz, 1 H), 6.10-6.19 (m, 1 H), 4.21-4.31 (m, 1 H), 4.00 (d, J = 7.06 Hz, 2 H), 3.91 and 3.92 (2s, 2CH3, 6 H), 3.54-3.65 (m, 1 H), 3.40-3.50 (m, 1 H), 3.22-3.38 (m, 2 H), 1.70-1.86 (m, 2 H), 1.55- 1.71 (m, 1 H), 1.29 (m, 2 H), 0.53- 0.66 (m, 2 H), 0.32-0.46 (m, 2 H). 3 Preparative HPLC (Method 1) 54

Free Base 728.1  6.12 (1) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 7.80-7.87 (m, 1 H), 7.68-7.80 (m, 3 H), 7.19 (d, J = 7.94 Hz, 1 H), 7.14 (d, J = 1.76 Hz, 1 H), 7.09 (t, J = 75.00 Hz, 1 H), 6.98 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 9.70, 4.41 Hz, 1 H), 4.18 (dd, J = 8.60, 4.19 Hz, 1 H), 3.91 (d, J = 7.06 Hz, 2 H), 3.47 (dd, J = 14.33, 9.92 Hz, 1 H), 3.35-3.41 (m, 1 H), 3.26 (dd, J = 14.11, 4.41 Hz, 1 H), 3.18 (dt, J = 9.70, 6.84 Hz, 1 H), 3.02 (s, 3 H), 2.89 (s, 3 H), 1.88-2.02 (m, 1 H), 1.60-1.73 (m, 2 H), 1.47-1.60 (m, 1 H), 1.13-1.28 (m, 1 H), 0.51-0.60 (m, 2 H), 0.26-0.40 (m, 2 H). 3 Flash Cromatography 55

Free Base 728.1  6.20 (1) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.79-7.87 (m, 1 H), 7.70-7.76 (m, 2 H), 7.67 (d, J = 7.50 Hz, 1 H), 7.21 (d, J = 8.38 Hz, 1 H), 7.13 (d, J = 1.76 Hz, 1 H), 7.10 (t, J = 75.00 Hz, 1 H), 6.96-7.03 (m, 1 H), 5.94-6.01 (m, 1 H), 4.13-4.25 (m, 1 H), 3.85-3.97 (m, 2 H), 3.34-3.53 (m, 2 H), 3.23-3.30 (m, 1 H), 3.12- 3.22 (m, 1 H), 3.00 (s, 3 H), 2.87 (s, 3 H), 1.86-2.01 (m, 1 H), 1.64- 1.83 (m, 2 H), 1.52-1.63 (m, 1 H), 1.13-1.29 (m, 1 H), 0.56 (dd, J = 7.94, 1.32 Hz, 2 H), 0.25-0.41 (m, 2 H).  +39.02 (c = 0.51; CHCl₃) 4 Preparative HPLC (Method 1) 56

Free Base 745.8  6.20; 6.30 (1)   41:59 5 Preparative HPLC (Method 1) 57

Free Base 674.1  7.15; 7.27 (1)   40:60 5 Preparative HPLC (Method 1) 58

Free Base 744.0  6.44; 6.35 (1)   40:60 5 Triturated with Et2O 59

Free Base 753.9  6.02; 6.22 (1)   36:64 5 Preparative HPLC (Method 1) 60

Free Base 693.0  7.52; 7.62 (1)   38:62 5 Preparative HPLC (Method 1) 61

Free Base 703.1  8.23; 8.32 (1)   37:63 5 Preparative HPLC (Method 1) 62

Free Base 681.0  7.17; 7.27 (1)   42:58 5 Preparative HPLC (Method 1) 63

Free Base 708.8  7.92; 8.02 (1)   38:62 5 Preparative HPLC (Method 1) 64

Free Base 678.9  6.35; 6.44 (1)   41:59 5 Preparative HPLC (Method 1) 65

Free Base 652.8  6.97; 7.12 (1)   51:49 5 Preparative HPLC (Method 1) 66

hydro- chloride 675.7  6.40; 6.48 (1)   38:62 5 Preparative HPLC (Method 1) 67

Free Base 710.9  7.63; 7.73 (1)   41:59 5 Preparative HPLC (Method 1) 68

Free Base 726.9  7.90; 7.98 (1)   40:60 5 Preparative HPLC (Method 1) 69

Free Base 706.7  7.95; 8.05 (1)   45:55 5 Preparative HPLC (Method 1) 70

Free Base 708.8  7.72; 7.80 (1)   39:61 5 Preparative HPLC (Method 1) 71

Free Base 680.9  7.87; 7.97 (1)   32:68 5 Preparative HPLC (Method 1) 72

Free Base 758.8  5.53; 5.63 (1)   37:63 5 Trituration with ethyl ether 73

Free Base 735.2  4.03; 4.09 (2)   60:40 5 Preparative HPLC (Method 1) 74

formate 761.2  3.97; 4.02 (2)   35:65 5 Preparative HPLC (Method 1) 75

Free Base 719.1  3.60 (2)   96:4 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 13.23-13.92 (bs, 1 H), 8.58 (s, 2 H), 8.20-8.41 (m, 2 H), 8.00- 8.17 (m, 1 H), 7.78 (m, 1 H), 7.17 (d, J = 8.38 Hz, 1 H), 7.04-7.14 (m, 2 H), 6.96 (d, J = 1.76 Hz, 1 H), 5.94-6.13 (m, 1 H), 5.46 (s, 1 H), 3.90 (d, J = 6.62 Hz, 2 H), 3.69 (m, 2 H), 3.42-3.54 (m, 1 H), 3.25-3.30 (m, 1 H), 2.89-3.03 (m, 1 H), 2.64-2.73 (m, 1 H), 1.11- 1.31 (m, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.33 (d, J = 4.85 Hz, 2 H). 5 Triturated with Et2O 76

Free Base 694.2  4.09; 4.13 (2)   33:67 5 Preparative HPLC (Method 1) 77

Free Base 751.8  5.62 (1) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 8.15 (m, 2 H), 7.96-8.02 (m, 1 H), 7.91 (m, 1 H), 7.65 (s, 2 H), 7.17 (m, 1 H), 7.05- 7.13 (m, 2 H), 6.94-7.04 (m, 1 H), 5.65-6.06 (m, 1 H), 4.37-4.50 (m, 1 H), 3.92 (d, J = 7.06 Hz, 2 H), 3.72-3.82 (m, 1 H), 3.57-3.68 (m, 1 H), 3.41-3.53 (m, 1 H), 3.19- 3.27 (m, 2 H), 3.09-3.18 (m, 1 H), 2.91-3.02 (m, 1 H), 2.78-2.89 (m, 1 H), 1.20-1.26 (m, 1 H), 0.49- 0.65 (m, 2 H), 0.35 (d, J = 5.73 Hz, 2 H). 8 Preparative HPLC (Method 1) 78

Free Base 744.0  5.84; 6.00 (1)   64:36 8 Preparative HPLC (Method 1) 79

Free Base 673.2  3.92; 3.93 (2)   67:33 8 Triturated with MeOH 80

Free Base 759.8  6.27; 6.45 (1)   47:53 13 Preparative HPLC (Method 1) 81

Free Base 781.8  6.52; 6.77 (1)   39:61 13 Preparative HPLC (Method 1) 82

Free Base 742.2  3.85 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.50 (s, 2 H), 7.57-7.84 (m, 4 H), 7.08-7.17 (m, 1 H), 7.02- 7.08 (m, 2 H), 6.83-6.93 (m, 1 H), 5.77-5.96 (m, 1 H), 4.56-4.73 (m, 1 H), 3.78-3.99 (m, 2 H), 3.56- 3.74 (m, 1 H), 3.33-3.46 (m, 2 H), 3.17-3.26 (m, 1 H), 2.99 (s, 3 H), 2.86 (s, 3 H), 1.99-2.17 (m, 1 H), 1.43-1.69 (m, 3 H), 1.08-1.31 (m, 2 H), 0.71-0.99 (m, 1 H), 0.43- 0.61 (m, 2 H), 0.25-0.38 (m, 2 H). 10 Preparative HPLC (Method 1) 83

Free Base 742.3  3.74 (2)   96:4 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.67-7.75 (m, 2 H), 7.56-7.64 (m, 1 H), 7.40- 7.50 (m, 1 H), 7.18-7.24 (m, 1 H), 7.05-7.13 (m, 2 H), 6.89-6.95 (m, 1 H), 5.92-6.00 (m, 1 H), 4.68- 4.80 (m, 1 H), 3.85-4.02 (m, 2 H), 3.54-3.66 (m, 1 H), 3.36-3.48 (m, 2 H), 3.16-3.26 (m, 1 H), 2.97 (s, 3 H), 2.81 (s, 3 H), 1.88-2.02 (m, 1 H), 1.38-1.64 (m, 4 H), 1.11- 1.29 (m, 2 H), 0.65-0.80 (m, 1 H), 0.50-0.64 (m, 2 H), 0.29-0.42 (m, 2 H).  +16.33 (c = 0.24; CHCl3) 9 Preparative HPLC (Method 1) 84

Free Base 746.1  6.30 (1) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.85-7.99 (m, 2 H), 7.65-7.79 (m, 2 H), 7.13- 7.22 (m, 2 H), 7.09 (t, J = 75.00 Hz, 1 H), 6.98 (dd, J = 8.38, 1.76 Hz, 1 H), 6.00 (dd, J = 9.26, 4.41 Hz, 1 H), 4.89 (dd, J = 7.28, 4.63 Hz, 1 H), 4.73 (d, J = 10.58 Hz, 1 H), 4.32 (d, J = 10.58 Hz, 1 H), 3.92 (d, J = 7.06 Hz, 2 H), 3.46 (dd, J = 14.11, 9.70 Hz, 1 H), 3.23-3.30 (m, 1 H), 2.93-3.08 (m, 5 H), 2.88 (s, 3 H), 1.23 (d, J = 7.06 Hz, 1 H), 0.49-0.64 (m, 2 H), 0.33 (q, J = 4.85 Hz, 2 H). 11 Preparative HPLC (Method 1) 85

Free Base 680.8  7.07; 7.18 (1)   36:64 5 Triturated with Et2O 86

Free Base 657.3  4.09 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.61 (s, 2 H), 7.69-7.82 (m, 3 H), 7.60-7.68 (m, 2 H), 7.19 (d, J = 7.94 Hz, 1 H), 7.14 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.98 (dd, J = 8.38, 1.76 Hz, 1 H), 6.02 (dd, J = 9.70, 4.41 Hz, 1 H), 4.13 (dd, J = 8.60, 4.19 Hz, 1 H), 3.92 (d, J = 6.62 Hz, 2 H), 3.47 (dd, J = 14.11, 9.70 Hz, 1 H), 3.33-3.41 (m, 1 H), 3.26 (dd, J = 14.11, 4.41 Hz, 1 H), 3.16 (ddd, J = 9.81, 6.84, 6.73 Hz, 1 H), 1.83-1.98 (m, 1 H), 1.58-1.74 (m, 2 H), 1.41-1.57 (m, 1 H), 1.14-1.27 (m, 1 H), 0.48-0.63 (m, 2 H), 0.26-0.40 (m, 2 H) 3 No purification 87

Free Base 739.1  4.30; 4.25 (2)   32:68 5 Preparative HPLC (Method 1) 88

Free Base 676.2  3.62 (2)   99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 9.05 (d, J = 2.20 Hz, 1 H), 8.91 (dd, J = 4.63, 1.54 Hz, 1 H), 8.58 (s, 2 H), 8.31 (ddd, J = 8.27, 1.87, 1.76 Hz, 1 H), 7.69 (dd, J = 8.38, 4.85 Hz, 1 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.05-7.14 (m, 2 H), 6.95 (dd, J = 8.16, 1.54 Hz, 1 H), 6.01 (dd, J = 9.04, 5.07 Hz, 1 H), 5.63 (s, 1 H), 3.80-3.96 (m, 3 H), 3.61-3.72 (m, 1 H), 3.46 (dd, J = 14.11, 9.26 Hz, 1 H), 3.28-3.40 (m, 2 H), 2.91-3.04 (m, 1 H), 2.69 (ddd, J = 11.14, 6.39, 6.28 Hz, 1 H), 1.21 (ddd, J = 12.13, 7.50, 4.63 Hz, 1 H), 0.49-0.64 (m, 2 H), 0.26-0.41 (m, 2 H).  −43.74 (c = 0.53; CHCl₃) 6 Preparative HPLC (Method 1) 89

Free Base 675.2  4.20 (2)   97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 7.87 (d, J = 7.50 Hz, 2 H), 7.75 (d, J = 7.50 Hz, 1 H), 7.61-7.70 (m, 2 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.05- 7.14 (m, 2 H), 6.96 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 9.26, 4.85 Hz, 1 H), 5.43 (s, 1 H), 3.90 (d, J = 7.06 Hz, 2 H), 3.75-3.85 (m, 1 H), 3.59-3.68 (m, 1 H), 3.44 (d, J = 9.26 Hz, 1 H), 3.29 (m, 1 H), 2.91-3.00 (m, 1 H), 2.64 (d, J = 11.03 Hz, 1 H), 1.18 (d, J = 7.06 Hz, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.26-0.40 (m, 2 H).  −37.96 (c = 0.56; CHCl₃) 6 Flash Cromatography 90

Free Base 679.2  3.61 (2)   99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.52 (m, 1 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.10- 7.16 (m, 2 H), 7.09 (t, J = 75.00 Hz, 1 H), 6.97 (dd, J = 8.38, 1.76 Hz, 1 H), 6.02 (dd, J = 9.26, 4.85 Hz, 1 H), 5.49 (s, 1 H), 3.86-3.99 (m, 6 H), 3.71-3.80 (m, 1 H), 3.43 (dd, J = 14.11, 9.70 Hz, 1 H), 3.25-3.31 (m, 1 H), 2.92-3.10 (m, 2 H), 1.15-1.30 (m, 1 H), 0.49- 0.65 (m, 2 H), 0.29-0.42 (m, 2 H).  −43.30 (c = 0.48; CHCl₃) 6 Preparative HPLC (Method 1) 91

Free Base 754.1  3.58 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 8.28 (m, 1 H), 8.14 (dd, J = 15.66, 8.16 Hz, 2 H), 7.87 (t, J = 7.94 Hz, 1 H), 7.56- 7.72 (m, 2 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.06-7.15 (m, 2 H), 6.96 (dd, J = 8.38, 1.76 Hz, 1 H), 6.03 (dd, J = 8.82, 5.29 Hz, 1H), 5.50 (s, 1 H), 3.85-3.99 (m, 2 H), 3.65- 3.82 (m, 2 H), 3.47 (dd, J = 14.11, 8.82 Hz, 1 H), 3.25-3.30 (m, 1 H), 2.94-3.05 (m, 1 H), 2.63-2.78 (m, 1 H), 1.13-1.32 (m, 1 H), 0.46- 0.63 (m, 2 H), 0.26-0.43 (m, 2 H). 6 Preparative HPLC (Method 1) 92

Free Base 753.1  3.70; 3.77 (2)   27:73 5 Preparative HPLC (Method 1) 93

Free Base 735.2  4.12 (2)   97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.45 (dd, J = 8.38, 2.21 Hz, 1 H), 7.32 (d, J = 1.76 Hz, 1 H), 7.15-7.21 (m, 2 H), 7.11 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.95 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 9.26, 4.85 Hz, 1 H), 5.51 (s, 1 H), 3.77-3.95 (m, 9 H), 3.54-3.66 (m, 1 H), 3.45 (dd, J = 14.11, 9.26 Hz, 1 H), 3.25-3.28 (m, 1 H), 2.87- 3.00 (m, 1 H), 2.52-2.64 (m, 1 H), 1.19-1.28 (m, 1 H), 0.47-0.65 (m, 2 H), 0.27-0.39 (m, 2 H). 6 No purification 94

Free Base 768.1  4.00 (2)   99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 8.07-8.16 (m, 2 H), 7.94-8.05 (m, 2 H), 7.71- 7.84 (bs, 1 H), 7.14-7.21 (m, 1 H), 7.08 (m, 2 H), 6.91-6.99 (m, 1 H), 5.92-6.11 (m, 1 H), 5.51 (s, 1 H), 3.90 (d, J = 7.06 Hz, 2 H), 3.76- 3.85 (m, 1 H), 3.63-3.74 (m, 1 H), 3.40-3.52 (m, 1 H), 3.25-3.35 (m, 1 H), 2.92-3.07 (m, 1 H), 2.63- 2.80 (m, 1 H), 2.48 (s, 3 H), 1.13- 1.30 (m, 1 H), 0.49-0.63 (m, 2 H), 0.26-0.40 (m, 2 H). 6 Preparative HPLC (Method 1) 95

Free Base 665.2  4.19 (2)   99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 8.06-8.11 (m, 1 H), 7.32-7.41 (m, 1 H), 7.15- 7.22 (m, 1 H), 7.06-7.14 (m, 2 H), 6.94-7.01 (m, 1 H), 6.76-6.82 (m, 1 H), 5.95-6.07 (m, 1 H), 5.33 (s, 1 H), 3.84-3.98 (m, 2 H), 3.67- 3.83 (m, 2 H), 3.39-3.53 (m, 1 H), 3.24-3.29 (m, 1 H), 2.98-3.09 (m, 1 H), 2.77-2.88 (m, 1 H), 1.16- 1.29 (m, 1 H), 0.52-0.63 (m, 2 H), 0.29-0.40 (m, 2 H). 6 Preparative HPLC (Method 1) 96

Free Base 665.2  4.13 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 8.45-8.52 (m, 1 H), 7.89-8.00 (m, 1 H), 7.15- 7.22 (m, 1 H), 7.05-7.14 (m, 2 H), 6.93-7.01 (m, 2 H), 5.92-6.09 (m, 1 H), 5.45 (s, 1 H), 3.84-3.96 (m, 2 H), 3.60-3.82 (m, 2 H), 3.37- 3.52 (m, 2 H), 2.94-3.09 (m, 1 H), 2.79-2.89 (m, 1 H), 1.13-1.32 (m, 1 H), 0.48-0.65 (m, 2 H), 0.26- 0.42 (m, 2 H). 6 Preparative HPLC (Method 1) 97

Free Base 782.1  4.35 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 8.23 (m, 1 H), 8.11 (m, 2 H), 7.95 (m, 1 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.11 (d, J = 2.20 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.91-6.98 (m, 1 H), 5.95-6.06 (m, 1 H), 5.61 (s, 1 H), 3.90 (dd, J = 7.06, 1.32 Hz, 3 H), 3.61-3.72 (m, 1 H), 3.42-3.51 (m, 1 H), 3.26-3.31 (m, 1 H), 2.92- 3.05 (m, 1 H), 2.62-2.75 (m, 7 H), 1.14-1.28 (m, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.33 (dd, J = 4.63, 1.10 Hz, 2 H). 6 Preparative HPLC (Method 1) 98

Free Base 731.2  4.52 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.62 (s, 2 H), 7.20 (m, 2 H), 7.12-7.17 (m, 1 H), 7.07 (d, J = 2.21 Hz, 3 H), 6.86-6.93 (m, 1 H), 5.81-5.96 (m, 1 H), 4.53-4.70 (m, 1 H), 3.85 (m, 5 H), 3.80 (s, 3 H), 3.51-3.65 (m, 1 H), 3.35-3.47 (m, 1 H), 3.17-3.28 (m, 1 H), 2.93- 3.06 (m, 1 H), 1.97-2.10 (m, 1 H), 1.40-1.64 (m, 3 H), 1.12-1.29 (m, 2 H), 0.80-0.99 (m, 1 H), 0.50- 0.62 (m, 2 H), 0.25-0.40 (m, 2 H). 10 Preparative HPLC (Method 1) 99

Free Base 672.3  4.17 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.78-8.86 (m, 2 H), 8.66 (s, 2 H), 7.99-8.11 (m, 1 H), 7.55- 7.65 (m, 1 H), 7.11-7.21 (m, 1 H), 7.02-7.10 (m, 2 H), 6.84-6.93 (m, 1 H), 5.83-5.92 (m, 1 H), 4.65- 4.76 (m, 1 H), 3.79-3.96 (m, 2 H), 3.62-3.74 (m, 1 H), 3.35-3.47 (m, 1 H), 3.18-3.26 (m, 1 H), 2.86- 3.05 (m, 1 H), 2.05-2.17 (m, 1 H), 1.46-1.74 (m, 3 H), 1.12-1.32 (m, 2 H), 0.80-0.98 (m, 1 H), 0.50- 0.63 (m, 2 H), 0.26-0.41 (m, 2 H). 10 Preparative HPLC (Method 1) 100

Free Base 733.1  4.54 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 8.17 (d, J = 8.38 Hz, 2 H), 8.03 (m, 2 H), 7.15-7.20 (m, 1 H), 7.05-7.13 (m, 2 H), 6.92-6.98 (m, 1 H), 5.93- 6.09 (m, 1 H), 5.49 (s, 1 H), 3.91 (m, 5 H), 3.77-3.86 (m, 1 H), 3.64-3.72 (m, 1 H), 3.41-3.51 (m, 1 H), 3.26-3.30 (m, 1 H), 2.91- 3.03 (m, 1 H), 2.64-2.77 (m, 1 H), 1.14-1.29 (m, 1 H), 0.51-0.60 (m, 2 H), 0.28-0.37 (m, 2 H). 6 Preparative HPLC (Method 1) 101

Free Base 733.1  4.44 (2)   96:4 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.96-8.04 (m, 1 H), 7.71-7.84 (m, 2 H), 7.62- 7.69 (m, 1 H), 7.13-7.20 (m, 1 H), 7.05-7.12 (m, 2 H), 6.91-6.98 (m, 1 H), 5.92-6.02 (m, 1 H), 5.68 (s, 1 H), 3.96-4.06 (m, 1 H), 3.86- 3.92 (m, 2 H), 3.84 (s, 3 H), 3.56- 3.67 (m, 1 H), 3.39-3.51 (m, 1 H), 3.24-3.29 (m, 1 H), 2.95-3.06 (m, 1 H), 2.74-2.84 (m, 1 H), 1.16- 1.27 (m, 1 H), 0.51-0.63 (m, 2 H), 0.29-0.37 (m, 2 H). 6 Preparative HPLC (Method 1) 102

Free Base 746.2  4.12 (2)   99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.92-7.98 (m, 1 H), 7.84-7.91 (m, 1 H), 7.63- 7.77 (m, 2 H), 7.18-7.25 (m, 1 H), 7.12-7.17 (m, 1 H), 7.09 (t, J = 75.00 Hz, 1 H), 6.96-7.03 (m, 1 H), 5.95-6.02 (m, 1 H), 4.92-5.04 (m, 1 H), 4.67-4.78 (m, 1 H), 4.25-4.34 (m, 1 H), 3.86-4.00 (m, 2 H), 3.42-3.56 (m, 1 H), 3.21- 3.29 (m, 1 H), 3.00 (m, 4 H), 2.86 (m, 4 H), 1.14-1.29 (m, 1 H), 0.50-0.63 (m, 2 H), 0.28-0.39 (m, 2 H). 12 Preparative HPLC (Method 1) 103

Free Base 705.2  4.80 (2)   97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.53-7.60 (m, 1 H), 7.40-7.46 (m, 1 H), 7.29- 7.37 (m, 2 H), 7.16-7.20 (m, 1 H), 7.09-7.12 (m, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.93-6.98 (m, 1 H), 5.96-6.07 (m, 1 H), 5.50 (s, 1 H), 3.88-3.94 (m, 2 H), 3.87 (s, 3 H), 3.77-3.85 (m, 1 H), 3.59-3.67 (m, 1 H), 3.40-3.50 (m, 1 H), 3.25-3.30 (m, 1 H), 2.91-3.02 (m, 1 H), 2.61-2.70 (m, 1 H), 1.15- 1.29 (m, 1 H), 0.53-0.61 (m, 2 H), 0.29-0.38 (m, 2 H) 6 Trituration with Et2O 104

Free Base 759.1  5.20 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.89-7.98 (m, 2 H), 7.80 (d, J = 5.29 Hz, 2 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.07- 7.13 (m, 2 H), 6.95 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 8.82, 5.29 Hz, 1 H), 5.62 (s, 1 H), 3.79- 3.97 (m, 3 H), 3.58-3.73 (m, 1 H), 3.41-3.53 (m, 1 H), 3.29 (d, J = 4.85 Hz, 1 H), 2.90-3.03 (m, 1 H), 2.62-2.74 (m, 1 H), 1.14-1.31 (m, 1 H), 0.48-0.65 (m, 2 H), 0.26- 0.41 (m, 2 H). 6 No purification 105

Free Base 761.2  4.74 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 8.45-8.50 (m, 1 H), 7.83-7.93 (m, 1 H), 7.14- 7.21 (m, 1 H), 7.04-7.12 (m, 2 H), 6.89-6.99 (m, 2 H), 5.92-6.05 (m, 1 H), 5.46 (s, 1 H), 3.85-3.94 (m, 2 H), 3.75-3.84 (m, 1 H), 3.66 (d, J = 9.26 Hz, 9 H), 3.39-3.49 (m, 1 H), 3.18-3.28 (m, 1 H), 2.90-3.03 (m, 1 H), 2.59-2.74 (m, 1 H), 1.13-1.30 (m, 1 H), 0.48-0.60 (m, 2 H), 0.26-0.38 (m, 2 H). 6 Preparative HPLC (Method 1) 106

Free Base 719.2  5.12 (2)   97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.64 (d, J = 7.94 Hz, 1 H), 7.17 (d, J = 8.38 Hz, 1 H), 7.10 (dd, J = 6.39, 2.43 Hz, 3 H), 6.95 (m, 2 H), 5.89-6.09 (m, 1 H), 5.51 (s, 1 H), 3.83-4.00 (m, 5 H), 3.62-3.79 (m, 1 H), 3.51-3.62 (m, 1 H), 3.36-3.48 (m, 1 H), 3.22-3.31 (m, 1 H), 2.93- 3.04 (m, 1 H), 2.63-2.81 (m, 1 H), 2.39 (s, 3 H), 1.15-1.31 (m, 1 H), 0.51-0.65 (m, 2 H), 0.33 (d, J = 4.85 Hz, 2 H). 6 Preparative HPLC (Method 1) 107

Free Base 710.1  4.79 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.16-7.23 (m, 1 H), 7.07-7.14 (m, 2 H), 6.94- 7.00 (m, 1 H), 5.87-6.14 (m, 1 H), 5.31 (s, 1 H), 3.84-3.97 (m, 2 H), 3.73 (m, 2 H), 3.40-3.58 (m, 1 H), 3.19-3.28 (m, 1 H), 2.88-3.15 (m, 2 H), 2.69 (s, 3 H), 2.55 (s, 3 H), 1.14-1.31 (m, 1 H), 0.51-0.64 (m, 2 H), 0.26-0.42 (m, 2 H). 6 Preparative HPLC (Method 1) 108

Free Base 746.2  5.13 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.11 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 7.03 (m, 1 H), 7.00 (d, J = 2.21 Hz, 1 H), 6.93-6.98 (m, 1 H), 6.86 (d, J = 8.38 Hz, 1 H), 5.92- 6.09 (m, 1 H), 5.42 (s, 1 H), 4.32 (m, 2 H), 3.90 (d, J = 6.17 Hz, 2 H), 3.69-3.84 (m, 1 H), 3.56-3.66 (m, 1 H), 3.33-3.53 (m, 3 H), 3.24-3.29 (m, 1 H), 2.91 (m, 4 H), 2.59-2.68 (m, 1 H), 1.15-1.27 (m, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.33 (d, J = 5.73 Hz, 2 H). 6 Preparative HPLC (Method 1) 109

Free Base 753.1  5.40 (2) >99:1 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.60 (s, 2 H), 8.17 (d, J = 10.58 Hz, 4 H), 7.15-7.21 (m, 1 H), 7.05-7.14 (m, 2 H), 6.93-7.00 (m, 1 H), 5.96-6.08 (m, 1 H), 5.54 (s, 1 H), 3.86-3.97 (m, 2 H), 3.76- 3.84 (m, 1 H), 3.62-3.74 (m, 1 H), 3.39-3.53 (m, 1 H), 3.35 (s, 3 H), 3.24-3.31 (m, 1 H), 2.91-3.05 (m, 1 H), 2.69-2.82 (m, 1 H), 1.13- 1.27 (m, 1 H), 0.47-0.65 (m, 2 H), 0.25-0.44 (m, 2 H). 6 Crystallized from EtOH/iprOH 110

Free Base 705.1  4.41 (2)   97:3 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.60 (s, 2 H), 7.80 (d, J = 9.26 Hz, 2 H), 7.13-7.22 (m, 3 H), 7.11 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.93-6.99 (m, 1 H), 5.95-6.07 (m, 1 H), 5.39 (s, 1 H), 3.84-3.94 (m, 5 H), 3.72- 3.82 (m, 1 H), 3.54-3.65 (m, 1 H), 3.40-3.50 (m, 1 H), 3.20-3.29 (m, 1 H), 2.89-2.99 (m, 1 H), 2.57- 2.70 (m, 1 H), 1.14-1.27 (m, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.33 (dd, J = 4.63, 1.54 Hz, 2 H). 6 Flash Cromatography 111

Free Base 752.2  4.36 (2)   98:2 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.63 (s, 2 H), 8.24 (d, J = 2.65 Hz, 1 H), 7.64 (dd, J = 9.26, 2.65 Hz, 1 H), 7.16 (d, J = 8.38 Hz, 1 H), 7.04-7.09 (m, 2 H), 6.80-6.95 (m, 2 H), 5.89 (dd, J = 8.82, 4.85 Hz, 1 H), 4.61 (d, J = 3.97 Hz, 1 H), 3.88 (t, J = 6.62 Hz, 2 H), 3.67-3.75 (m, 4 H), 3.59-3.65 (m, 4 H), 3.50-3.58 (m, 1 H), 3.35-3.46 (m, 1 H), 3.22 (dd, J = 14.11, 5.29 Hz, 1 H), 2.96 (d, J = 2.65 Hz, 1 H), 2.07 (m, 1 H), 1.57-1.70 (m, 1 H), 1.51 (d, J = 11.03 Hz, 2 H), 1.15-1.35 (m, 2 H), 0.80-0.96 (m, 1 H), 0.49-0.62 (m, 2 H), 0.28-0.41 (m, 2 H). 10 Preparative HPLC (Method 1) 112

Free Base 716.1  4.66 (2)   98:2 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.62 (s, 2 H), 8.37 (d, J = 8.82 Hz, 2 H), 7.97 (d, J = 8.82 Hz, 2 H), 7.14 (m, 1 H), 7.06 (m, 2 H), 6.83-6.92 (m, 1 H), 5.84- 5.96 (m, 1 H), 4.64-4.75 (m, 1 H), 3.86 (m, 2 H), 3.64-3.75 (m, 1 H), 3.35-3.47 (m, 1 H), 3.16-3.27 (m, 1 H), 2.90-3.05 (m, 1 H), 2.08- 2.17 (m, 1 H), 1.49-1.70 (m, 3 H), 1.13-1.31 (m, 2 H), 0.78-0.98 (m, 1 H), 0.48-0.66 (m, 2 H), 0.32 (m, 2 H). 10 Preparative HPLC (Method 1) 113

Free Base 778.2  4.45 (2)   98:2 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.60 (s, 2 H), 7.99-8.06 (m, 2 H), 7.97 (d, J = 1.76 Hz, 1 H), 7.80-7.90 (m, 1 H), 7.14 (d, J = 8.38 Hz, 1 H), 7.07 (t, J = 75.00 Hz, 1 H), 7.04 (d, J = 1.76 Hz, 1 H), 6.83-6.90 (m, 1 H), 5.85 (dd, J = 8.38, 5.29 Hz, 1 H), 4.73 (d, J = 4.41 Hz, 1 H), 3.86 (t, J = 7.50 Hz, 2 H), 3.63-3.74 (m, 1 H), 3.36-3.46 (m, 1 H), 3.18-3.26 (m, 1 H), 2.94 (m, 1 H), 2.65 (s, 6 H), 2.09-2.19 (m, 1 H), 1.54 (d, J = 15.88 Hz, 3 H), 1.19 (d, J = 4.85 Hz, 2 H), 0.78-0.98 (m, 1 H), 0.48-0.63 (m, 2 H), 0.26-0.40 (m, 2 H). 10 Preparative HPLC (Method 1) 114

Free Base 671.2  4.44 (2)   99:1 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.64 (s, 2 H), 7.62-7.70 (m, 3 H), 7.57 (d, J = 7.50 Hz, 2 H), 7.15 (m, 1 H), 7.02-7.10 (m, 2 H), 6.89 (m, 1 H), 5.84-5.91 (m, 1 H), 4.56-4.66 (m, 1 H), 3.87 (m, 2 H), 3.57-3.67 (m, 1 H), 3.36-3.48 (m, 1 H), 3.16-3.27 (m, 1 H), 2.90- 3.08 (m, 1 H), 1.98-2.12 (m, 1 H), 1.41-1.66 (m, 3 H), 1.10-1.30 (m, 2 H), 0.78-0.98 (m, 1 H), 0.57 (m, 2 H), 0.33 (dd, J = 4.85, 1.32 Hz, 2 H). 10 Preparative HPLC (Method 1) 115

Free Base 735.1  4.30 (2)   98:2 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.56 (s, 2 H), 7.15-7.33 (m, 4 H), 7.11 (m, 1 H), 7.09 (t, J = 75.00 Hz, 1 H), 6.92-6.99 (m, 1 H), 5.95-6.11 (m, 1 H), 5.59 (s, 1 H), 3.87-3.97 (m, 2 H), 3.85 (s, 3 H), 3.78 (m, 4 H), 3.52-3.63 (m, 1 H), 3.37-3.50 (m, 1 H), 3.28 (m, 1 H), 2.94-3.04 (m, 1 H), 2.67-2.80 (m, 1 H), 1.15-1.30 (m, 1 H), 0.52-0.60 (m, 2 H), 0.28-0.41 (m, 2 H). 6 Preparative HPLC (Method 1) 116

Free Base 675.3  3.79 (2)   98:2 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.55 (s, 2 H), 7.42 (m, 1 H), 7.12-7.20 (m, 1 H), 7.07 (d, J = 1.32 Hz, 2 H), 6.99 (d, J = 0.88 Hz, 1 H), 6.84-6.95 (m, 1 H), 5.86- 5.96 (m, 1 H), 4.56-4.65 (m, 1 H), 3.87 (m, 2 H), 3.78 (s, 3 H), 3.60- 3.69 (m, 1 H), 3.36-3.47 (m, 1 H), 3.17-3.26 (m, 1 H), 3.00-3.14 (m, 1 H), 2.03-2.13 (m, 1 H), 1.68-1.86 (m, 1 H), 1.43-1.64 (m, 2 H), 1.25-1.43 (m, 1 H), 1.11-1.24 (m, 1 H), 0.84-1.01 (m, 1 H), 0.47- 0.62 (m, 2 H), 0.28-0.40 (m, 2 H). 10 No purification 117

Free Base 717.1  4.06 (2) >99:1 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.58 (s, 2 H), 8.26-8.36 (m, 2 H), 8.10-8.16 (m, 1 H), 7.77- 7.86 (m, 1 H), 7.15-7.21 (m, 1 H), 7.10-7.14 (m, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.92-6.98 (m, 1 H), 5.97-6.06 (m, 1 H), 5.56 (s, 1 H), 3.87-3.94 (m, 2 H), 3.75-3.86 (m, 1 H), 3.63-3.72 (m, 1 H), 3.42-3.51 (m, 1 H), 3.38 (d, J = 7.06 Hz, 1 H), 2.91-3.03 (m, 1 H), 2.68 (m, 4 H), 1.15-1.33 (m, 1 H), 0.50-0.62 (m, 2 H), 0.27-0.41 (m, 2 H). 6 No purification 118

Free Base 768.1  3.75; 3.84 (2)   22:78 6 Preparative HPLC (Method 1) 119

Free Base 679.2  3.28 (2) >99:1 ¹H NMR (400 MHz, DMSO-d6) δ ppm 8.56 (s, 2 H), 7.93 (m, 1 H), 7.87 (m, 1 H), 7.17 (m, 1 H), 7.10 (d, J = 9.70 Hz, 2 H), 6.92-6.98 (m, 1 H), 5.94-6.11 (m, 1 H), 5.35 (s, 1 H), 3.91 (d, J = 7.06 Hz, 2 H), 3.73 (m, 4 H), 3.61-3.71 (m, 1 H), 3.40-3.49 (m, 1 H), 3.23-3.30 (m, 1 H), 2.94-3.04 (m, 1 H), 2.76-2.88 (m, 1 H), 1.16-1.28 (m, 1 H), 0.56 (d, J = 7.94 Hz, 2 H), 0.34 (d, J = 4.41 Hz, 2 H). 6 Preparative HPLC (Method 1) 121

Free Base 757.1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.70-7.82 (m, 3 H), 7.66-7.70 (m, 1 H), 7.13- 7.20 (m, 1 H), 7.06 (t, J = 75.00 Hz, 2 H), 6.92-6.99 (m, 1 H), 5.89-6.07 (m, 1 H), 3.83-3.93 (m, 2 H), 3.34-3.48 (m, 2 H), 3.16- 3.24 (m, 2 H), 2.95-3.07 (m, 3 H), 2.89 (m, 7 H), 2.42-2.48 (m, 4 H), 1.13-1.26 (m, 1 H), 0.49-0.62 (m, 2 H), 0.28-0.38 (m, 2 H). na 14 Preparative HPLC (Method 1) 200

Free Base 699.98  4.03 (3)   95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.55 (s, 2 H), 8.12-8.21 (m, 1 H), 8.04-8.12 (m, 1 H), 7.96 (td, 1 H), 7.91 (td, 1 H), 7.17 (d, 1 H), 7.10 (d, 1 H), 6.94 (dd, 1 H), 7.08 (t, 1 H), 5.94 (dd, 1 H), 5.62 (s, 1 H), 3.93-4.00 (m, 1 H), 3.90 (d, 2 H), 3.67-3.73 (m, 1 H), 3.44 (dd, 1 H), 3.27 (dd, 1 H), 3.07 (ddd, 1 H), 2.90 (dt, 1 H), 1.12-1.29 (m, 1 H), 0.46-0.66 (m, 2 H), 0.18-0.42 (m, 2 H)  −56.05 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 201

Free Base 732.96  4.12 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.56 (s, 2 H), 7.29-7.36 (m, 2 H), 7.18 (d, 1 H), 7.07-7.14 (m, 2 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.41 (s, 1 H), 4.27- 4.47 (m, 4 H), 3.91 (d, 2 H), 3.77 (dt, 1 H), 3.61 (dt, 1 H), 3.46 (dd, 1 H), 3.32-3.35 (m, 1 H), 2.97 (dt, 1 H), 2.69 (ddd, 1 H), 1.10-1.36 (m, 1 H), 0.48-0.68 (m, 2 H), 0.22- 0.43 (m, 2 H)  −50.2 (c = 0.44, DCM) 6 Chromatogrphy on silica gel followed by treatment with polymer supported carbonate in DCM/CH₃CN, filtration and evaporation 202

Free Base 714.01  4.18 (3) >95:5 (¹H NMR B) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.53 (s, 2 H), 8.03 (d, 1 H), 7.96 (d, 1 H), 7.72 (dd, 1 H), 7.17 (d, 1 H), 7.10 (d, 1 H), 6.94 (dd, 1 H), 7.08 (t, 1 H), 5.98 (dd, 1 H), 5.67 (s, 1 H), 3.94 (ddd, 1 H), 3.83-3.92 (m, 2 H), 3.65 (dt, 1 H), 3.45 (dd, 1 H), 3.29 (dd, 1 H), 3.07 (ddd, 1 H), 2.86 (dt, 1 H), 2.50 (s, 3 H), 1.11-1.30 (m, 1 H), 0.50-0.66 (m, 2 H), 0.27-0.40 (m, 2 H)  −81.2 (c = 0.7, DCM) 6 Chromatography on silca gel followed by preparative HPLC (Method 2) 203

Free Base 709.02  4.41 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.19 (d, 1 H), 7.12 (d, 1 H), 6.98 (s, 1 H), 6.97 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.40 (s, 1 H), 3.91 (d, 2 H), 3.78 (dt, 1 H), 3.62 (dt, 1 H), 3.45 (dd, 1 H), 3.30 (dd, 1 H), 3.03 (dt, 1 H), 2.80 (dt, 1 H), 2.57 (s, 3 H), 2.40 (s, 3 H), 1.11-1.34 (m, 1 H), 0.45-0.70 (m, 2 H), 0.24-0.45 (m, 2 H)  −50.27 (c = 0.3, DCM) 6 Preparative HPLC (Method 2) 204

Free Base 786.87  4.68 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.88 (d, 1 H), 7.83 (d, 1 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.01 (dd, 1 H), 5.46 (s, 1 H), 3.91 (d, 2 H), 3.80-3.88 (m, 1 H), 3.68 (dt, 1 H), 3.44 (dd, 1 H), 3.30 (dd, 1 H), 3.06 (dt, 1 H), 2.91 (dt, 1 H), 2.42 (s, 3 H), 1.05-1.32 (m, 1 H), 0.47-0.66 (m, 2 H), 0.21- 0.47 (m, 2 H)  −74.95 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 205

Free Base 766.98  4.57 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 8.05 (d, 1 H), 7.79 (dd, 1 H), 7.63 (d, 1 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.56 (s, 1 H), 3.91 (d, 2 H), 3.82 (dt, 1 H), 3.59-3.69 (m, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.98 (dt, 1 H), 2.71 (dt, 1 H), 2.46 (s, 3 H), 1.07-1.34 (m, 1 H), 0.47-0.67 (m, 2 H), 0.24-0.47 (m, 2 H)  −58.39 (c = 1.5, DCM) 6 Preparative HPLC (Method 2) 206

Free Base 700.06  4.05 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 8.11-8.22 (m, 2 H), 7.98-8.11 (m, 2 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.56 (s, 1 H), 3.90 (d, 2 H), 3.84 (dt, 1 H), 3.67 (dt, 1 H), 3.46 (dd,1 H), 3.31 (dd, 1 H), 2.99 (dt, 1 H), 2.75 (dt, 1 H), 1.00-1.34 (m, 1 H), 0.47-0.66 (m, 2 H), 0.26-0.42 (m, 2 H)  −52.16 (c = 0.5, DCM) 6 Preparative HPLC (Method 2) 207

Free Base 700.1  4.02 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 8.44 (t, 1 H), 8.08-8.29 (m, 2 H), 7.85 (t, 1 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (dd, 1 H), 6.03 (dd, 1 H), 5.70 (s, 1 H), 3.90 (d, 2 H), 3.85 (t, 1 H), 3.67 (dt, 1 H), 3.47 (dd, 1 H), 3.32 (dd, 1 H), 2.89- 3.12 (m, 1 H), 2.59-2.79 (m, 1 H), 1.22 (m, 1 H), 0.46-0.77 (m, 2 H), 0.31-0.37 (m, 2 H)  −38.8 (c = 0.3, DCM) 6 Preparative HPLC (method 2) 208

Free Base 741.07  5.99 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.70 (d, 1 H), 8.59 (s, 2 H), 8.07-8.20 (m, 2 H), 7.93-8.06 (m, 2 H), 7.87 (d, 1 H), 7.18 (d, 1 H), 7.12 (d, 1 H), 6.97 (dd, 1 H), 7.08 (t, 1 H), 6.65 (dd, 1 H), 6.03 (dd, 1 H), 5.51 (s, 1 H), 3.91 (d, 2 H), 3.86 (dt, 1 H), 3.66 (dt, 1 H), 3.47 (dd, 1 H), 3.32 (dd, 1 H), 2.98 (dt, 1 H), 2.70 (dt, 1 H), 1.05-1.41 (m, 1 H), 0.45-0.67 (m, 2 H), 0.23- 0.45 (m, 2 H)  −50.75 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 209

Free Base 718.08  4.16 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57-8.63 (m, 0 H), 8.56 (s, 2 H), 8.18-8.36 (m, 0 H), 7.80 (t, 1 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 6.95 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 5.73 (s, 1 H), 3.90 (d, 2 H), 3.79-3.88 (m, 1 H), 3.59-3.74 (m, 1 H), 3.18-3.41 (m, 2 H), 2.91-3.05 (m, 1 H), 2.65-2.77 (m, 3 H), 1.01-1.34 (m, 1 H), 0.44- 0.66 (m, 2 H), 0.21-0.44 (m, 2 H) −108 (c = 0.7, DCM) 6 Preparative HPLC (Method 2) 210

Free Base 744.15  3.79 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.80 (dd, 1 H), 7.73 (d, 1 H), 7.19 (d, 1 H), 7.19 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 5.40 (s, 1 H), 3.91 (d, 2 H), 3.78 (dt, 1 H), 3.69 (s, 2 H), 3.58- 3.68 (m, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 3.18 (s, 3 H), 2.97 (dt, 1 H), 2.65-2.79 (m, 1 H), 1.02-1.37 (m, 1 H), 0.45-0.68 (m, 2 H), 0.27-0.45 (m, 2 H)  −61.80 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 211

Free Base 734.04  4.27 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.52 (s, 2 H), 8.19 (d, 1 H), 8.14 (d, 1 H), 8.03 (dd, 1 H), 7.17 (d, 1 H), 7.10 (d, 1 H), 6.94 (dd, 1 H), 7.08 (t, 1 H), 5.97 (dd, 1 H), 5.77 (s, 1 H), 3.95-4.11 (m, 1 H), 3.76-3.95 (m, 2 H), 3.67 (dt, 1 H), 3.45 (dd, 1 H), 3.29 (dd, 1 H), 3.08 (ddd, 1 H), 2.95 (dt, 1 H), 1.05-1.33 (m, 1 H), 0.46-0.69 (m, 2 H), 0.22-0.46 (m, 2 H)  −40.70 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 212

Free Base 745.17  4.79 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 8.13 (s, 1 H), 8.04 (d, 1 H), 7.88 (s, 1 H), 7.45 (dd, 1 H), 7.18 (d, 1 H), 7.12 (d, 1 H), 6.97 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 5.41 (s, 1 H), 3.91 (d, 2 H), 3.80 (t, 2 H), 3.47 (dd, 1 H), 3.32 (dd, 1 H), 3.04 (dt, 1 H), 2.89 (dt, 1 H), 2.47 (s, 3 H), 1.05- 1.36 (m, 1 H), 0.46-0.81 (m, 2 H), 0.07-0.46 (m, 2 H)  −72.10 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) 213

Free Base 755.21  4.15 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 8.03 (m, 2 H), 7.87 (m, 2 H), 7.82 (d, 1 H), 7.18 (d, 1 H), 7.12 (d, 1 H), 6.96 (dd, 1 H), 6.88 (d, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.45 (s, 1 H), 3.93 (s, 3 H), 3.91 (d, 2 H), 3.83 (dt, 1 H), 3.65 (dt, 1 H), 3.47 (dd, 1 H), 3.31 (dd, 1 H), 2.98 (dt, 1 H), 2.67 (dt, 1 H), 1.01-1.37 (m, 1 H), 0.46- 0.69 (m, 2 H), 0.20-0.44 (m, 2 H)  −53.00 (c = 0.7, DCM) 6 Preparative HPLC (Method 2) 214

Free Base 741.19  4.36 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.86-8.03 (m, 2 H), 7.37-7.44 (m, 2 H), 7.45 (t, 1 H), 7.19 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.47 (s, 1 H), 3.91 (d, 2 H), 3.80 (dt, 1 H), 3.65 (dt, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.98 (dt, 1 H), 2.70 (dt, 1 H), 1.04- 1.38 (m, 1 H), 0.46-0.68 (m, 2 H), 0.24-0.42 (m, 2 H)  −42.49 (c = 1.4, DCM) 6 Preparative HPLC (Method 2) 215

Free Base 777.16  4.68 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.53 (s, 2 H), 8.12 (d, 1 H), 8.08 (d, 1 H), 8.02 (dd, 1 H), 7.16 (d, 1 H), 7.09 (d, 1 H), 6.92 (dd, 1 H), 7.08 (t, 1 H), 5.94 (dd, 1 H), 5.61 (s, 1 H), 3.90-4.00 (m, 1 H), 3.90 (d, 2 H), 3.60-3.69 (m, 1 H), 3.43 (dd, 1 H), 3.26 (dd, 1 H), 3.02-3.19 (m, 2 H), 0.91-1.43 (m, 1 H), 0.44-0.85 (m, 2 H), 0.23- 0.44 (m, 2 H)  −48.29 (c = 0.7, DCM) 6 Preparative HPLC (Method 2) 216

Free Base 723.15 54.25 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.51-7.63 (m, 2 H), 7.31 (dd, 1 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 5.58 (s, 1 H), 3.91 (s, 3 H), 3.86-3.97 (m, 2 H), 3.71-3.84 (m, 1 H), 3.60 (dt, 1 H), 3.44 (dd, 1 H), 3.31 (dd, 1 H), 3.03 (ddd, 1 H), 2.78 (dt, 1 H), 1.04-1.35 (m, 1 H), 0.43-0.69 (m, 2 H), 0.24-0.43 (m, 2 H)  −26.09 (c = 1.6, DCM) 6 Preparative HPLC (Method 2) 217

Free Base 731.18  4.58 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 8.23 (s, 1 H), 8.14-8.20 (m, 1 H), 8.00-8.14 (m, 1 H), 7.50-7.68 (m, 2 H), 7.19 (d, 1 H), 7.12 (d, 1 H), 6.98 (dd, 1 H), 7.08 (t, 1 H), 6.04 (dd, 1 H), 5.43 (s, 1 H), 3.91 (d, 2 H), 3.81 (t, 2 H), 3.48 (dd, 1 H), 3.32 (dd, 1 H), 3.05 (dt, 1 H), 2.91 (dt, 1 H), 1.05-1.40 (m, 1 H), 0.45-0.66 (m, 2 H), 0.18-0.45 (m, 2 H)  −46.14 (c = 0.7, DCM) 6 Preparative HPLC (Method 2) 218

Free Base 732.18  3.66 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.79 (d, 1 H), 7.64 (dd, 1 H), 7.26 (d, 1 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.49 (s, 1 H), 3.90 (d, 2 H), 3.75- 3.88 (m, 1 H), 3.62 (dt, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.95 (dt, 1 H), 2.60-2.68 (m, 1 H), 0.97- 1.37 (m, 1 H), 0.45-0.71 (m, 2 H), 0.18-0.45 (m, 2 H)  −32.95 (c = 0.4, DCM) 6 Preparative HPLC (Method 2) followed by flash chromatography on silica gel and further preparative HPLC (Method 2) 219

Free Base 758  3.92 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.91-8.00 (m, 2 H), 7.80-7.91 (m, 2 H), 7.18 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.42 (s, 1 H), 3.91 (d, 2 H), 3.90 (t, 2 H), 3.81 (dt, 1 H), 3.63 (dt, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.97 (dt, 1 H), 2.64 (dt, 1 H), 2.57 (t, 2 H), 2.10 (quin, 2 H), 1.07- 1.38 (m, 1 H), 0.47-0.71 (m, 2 H), 0.22-0.41 (m, 2 H)  −65.83 (c = 1.8, DCM) 6 Preparative HPLC (Method 2) 220

Free Base 772.09  3.93 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.88 (d, 1 H), 7.69 (d, 1 H), 7.62 (dd, 1 H), 7.18 (d, 1 H), 7.12 (d, 1 H), 6.97 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 5.43 (s, 1 H), 3.91 (d, 2 H), 3.77- 3.84 (m, 1 H), 3.71-3.77 (m, 2 H), 3.64 (ddd, 1 H), 3.47 (dd, 1 H), 3.31 (dd, 1 H), 2.98 (dt, 1 H), 2.83 (t, 2 H), 2.68 (dt, 1 H), 2.25 (s, 3 H), 1.91 (quin, 2 H), 1.06-1.36 (m, 1 H), 0.45-0.68 (m, 2 H), 0.23- 0.45 (m, 2 H)  −67.13 (c = 0.6, DCM) 6 Preparative HPLC (Method 2) 221

Free Base 760.15  3.61 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.90 (t, 1 H), 7.70-7.85 (m, 2 H), 7.40-7.59 (m, 2 H), 7.18 (d, 1 H), 7.12 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.42 (s, 1 H), 3.91 (d, 2 H), 3.78 (dt, 1 H), 3.63 (dt, 1 H), 3.46 (dd, 1 H), 3.23-3.39 (m, 3 H), 2.96 (dt, 1 H), 2.83 (t, 2 H), 2.63 (dt, 1 H), 1.77 (s, 3 H), 1.05-1.48 (m, 1 H), 0.47-0.66 (m, 2 H), 0.25-0.47 (m, 2 H)  −51.61 (c = 1.6, DCM) 6 Preparative HPLC (Method 2) 222

Free Base 773.19  4.46 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.72-8.01 (m, 2 H), 7.25-7.32 (m, 2 H), 7.19 (d, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.02 (dd, 1 H), 5.44 (s, 1 H), 4.94 (q, 2 H), 3.91 (d, 2 H), 3.80 (dt, 1 H), 3.62 (dt, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.97 (dt, 1 H), 2.65 (dt, 1 H), 1.13- 1.35 (m, 1 H), 0.47-0.71 (m, 2 H), 0.25-0.40 (m, 2 H)  −51.04 (c = 0.50, DCM) 6 Trituration with EtOH 223

Free Base 689.17  4.26 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.53 (s, 2 H), 7.36-7.50 (m, 5 H), 7.17 (d, 1 H), 7.09 (d, 1 H), 6.94 (dd, 1 H), 7.07 (t, 1 H), 5.99 (dd, 1 H), 5.20 (s, 1 H), 4.61 (d, 1 H), 4.54 (d, 1 H), 3.86-3.96 (m, 2 H), 3.82 (dt, 1 H), 3.57 (dt, 1 H), 3.41 (dd, 1 H), 3.28 (dd, 1 H), 2.92-3.14 (m, 2 H), 1.05-1.37 (m, 1 H), 0.46-0.66 (m, 2 H), 0.18- 0.44 (m, 2 H)  −18.6 (c = 0.9, DCM) 6 Treatment with polymer supported isocyanate followed by preparative HPLC (Method 2) 224

Free Base 703  4.33 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.52 (s, 2 H), 7.20-7.41 (m, 5 H), 7.16 (s, 1 H), 7.11 (d, 1 H), 6.96 (dd, 1 H), 7.07 (t, 1 H), 6.03 (dd, 1 H), 5.59 (s, 1 H), 3.94-4.13 (m, 1 H), 3.91 (d, 2 H), 3.39-3.67 (m, 4 H), 3.28 (d, 1 H), 3.02-3.19 (m, 2 H), 2.97 (t, 2 H), 1.08-1.36 (m, 1 H), 0.47-0.68 (m, 2 H), 0.23-0.42 (m, 2 H)  −58.4 (c = 0.4 DCM) 6 Preparative (Method 3) 225

Free Base 671.24  4.06 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.33-7.46 (m, 5 H), 7.16 (d, 1 H), 7.10 (d, 1 H), 6.95 (dd, 1 H), 7.06 (t, 1 H), 5.98 (dd, 1 H), 4.48 (d, 1 H), 4.39 (d, 1 H), 4.03 (dd, 1 H), 3.91 (dd, 1 H), 3.87 (dd, 1 H), 3.42 (dd, 1 H), 3.30-3.37 (m, 2 H), 3.23 (dd, 1 H), 1.97-2.22 (m, 1 H), 1.75-1.92 (m, 1 H), 1.59-1.75 (m, 2 H), 1.08-1.32 (m, 1 H), 0.46-0.70 (m, 2 H), 0.14-0.40 (m, 2 H)  −14.55 (c = 0.22, DCM) 3 Flash chromatography on silica gel followed by trituration with MeOH 226

Free Base 744.11  3.72 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.81 (dd, 1 H), 7.73 (d, 1 H), 7.18 (d, 2 H), 7.15 (d, 1 H), 6.98 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 4.80 (dd, 1 H), 4.63 (d, 1 H), 4.31 (d, 1 H), 3.93 (d, 2 H), 3.67 (s, 2 H), 3.47 (dd, 1 H), 3.27 (dd, 1 H), 3.18 (s, 3 H), 3.03 (dd, 1 H), 2.96 (dd, 1 H), 1.10-1.36 (m, 1 H), 0.49-0.69 (m, 2 H), 0.24-0.42 (m, 2 H)  −95.8 (c = 0.52, DCM) 11 Preparative HPLC (Method 2) 227

Free Base 671.12  4.19 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.61-7.81 (m, 5 H), 7.18 (d, 1 H), 7.09 (d, 1 H), 6.96 (dd, 1 H), 7.07 (t, 1 H), 5.93 (dd, 1 H), 3.92 (d, 2 H), 3.45 (dd, 2 H), 3.31-3.37 (m, 1 H), 3.21 (dd, 1 H), 2.54-2.70 (m, 2 H), 2.30- 2.46 (m, 1 H), 1.80 (m, 1 H), 1.58- 1.74 (m, 1 H), 1.40-1.58 (m, 1 H), 1.27-1.40 (m, 1 H), 1.07-1.27 (m, 1 H), 0.46-0.71 (m, 2 H), 0.08- 0.46 (m, 2 H)  +1.349 (c = 0.43, MeOH) 15 Flash chromatogrphy on silica gel 228

Free Base 742.12  3.78 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2 H), 7.72-7.84 (m, 3 H), 7.70 (t, 1 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 6.96 (dd, 1 H), 7.07 (t, 1 H), 5.94 (dd, 1 H), 3.92 (d, 2 H), 3.47-3.59 (m, 1 H), 3.45 (dd, 1 H), 3.32-3.39 (m, 1 H), 3.21 (dd, 1 H), 3.02 (br. s., 3 H), 2.90 (br. s., 3 H), 2.55-2.69 (m, 2 H), 1.03- 1.96 (m, 6 H), 0.47-0.69 (m, 2 H), 0.20-0.47 (m, 2 H)  +2.018 (c = 0.565, MeOH) 15 Flash chromatogrphy on silica gel 229

Free Base 671.17  4.22 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.60-7.81 (m, 5 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 7.00 (dd, 1 H), 7.08 (t, 1 H), 5.93 (dd, 1 H), 3.93 (d, 2 H), 3.44 (dd, 1 H), 3.33-3.39 (m, 1 H), 3.21 (dd, 1 H), 3.06-3.17 (m, 1 H), 2.55- 2.86 (m, 3 H), 1.63-1.82 (m, 1 H), 1.29-1.63 (m, 3 H), 1.04-1.29 (m, 1 H), 0.47-0.72 (m, 2 H), 0.18- 0.43 (m, 2 H)  −25.04 (c = 0.46, MeOH) 16 Flash chromatogrphy on silica gel 230

Free Base 742.23  3.83 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.80 (dt, 1 H), 7.76 (dt, 1 H), 7.75 (t, 1 H), 7.70 (t, 1 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 6.99 (dd, 1 H), 7.08 (t, 1 H), 5.93 (dd, 1 H), 3.93 (d, 2 H), 3.44 (dd, 1 H), 3.35-3.42 (m, 1 H), 3.21 (dd, 1 H), 3.09-3.17 (m, 1 H), 3.01 (br. s., 3 H), 2.89 (br. s., 3 H), 2.79-2.88 (m, 1 H), 2.55-2.71 (m, 2 H), 1.65-1.86 (m, 1 H), 1.31- 1.65 (m, 3 H), 1.05-1.30 (m, 1 H), 0.49-0.66 (m, 2 H), 0.22-0.43 (m, 2 H)  −25.66 (c = 0.265, MeOH) 16 Flash chromatogrphy on silica gel 231

Free Base 673.15  3.96 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.53-7.87 (m, 5 H), 7.19 (d, 1 H), 7.12 (d, 1 H), 6.99 (dd, 1 H), 7.07 (t, 1 H), 5.95 (dd, 1 H), 4.38 (dd, 1 H), 3.88 (dt, 1 H), 3.93 (d, 2 H), 3.46-3.69 (m, 3 H), 3.08-3.29 (m, 2 H), 2.54- 2.61 (m, 2 H), 1.15-1.29 (m, 1 H), 0.49-0.71 (m, 2 H), 0.17-0.44 (m, 2 H)  +5.102 (c = 0.49, DCM) 17 Flash chromatogrphy on silica gel followed by preparative HPLC (Method 2) 232

Free Base 744.18  3.58 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.73-7.86 (m, 3 H), 7.67-7.73 (m, 1 H), 7.19 (d, 1 H), 7.12 (d, 1 H), 6.99 (dd, 1 H), 7.07 (t, 1 H), 5.96 (dd, 1 H), 4.39 (dd, 1 H), 3.93 (d, 2 H), 3.89 (dt, 1 H), 3.61 (ddd, 1 H), 3.50 (dd, 1 H), 3.38-3.48 (m, 1 H), 3.13-3.27 (m, 2 H), 3.03 (br. s., 3H), 2.91 (br. s., 3 H), 2.55-2.70 (m, 2 H), 1.06-1.37 (m, 1 H), 0.51-0.65 (m, 2 H), 0.30-0.42 (m, 2 H)  −9.114 (c = 0.7, DCM) 17 Trituration with EtOH 233

Free Base 673.29  3.97 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.60-7.84 (m, 5 H), 7.19 (d, 1 H), 7.11 (d, 1 H), 7.01 (dd, 1 H), 7.09 (t, 1 H), 5.92 (dd, 1 H), 4.38 (dd, 1 H), 3.93 (d, 2 H), 3.77 (ddd, 1 H), 3.53-3.69 (m, 1 H), 3.45 (dd, 1 H), 3.17-3.29 (m, 2 H), 3.02 (dd, 1 H), 2.86-2.98 (m, 1 H), 2.69-2.83 (m, 1 H), 1.07-1.40 (m, 1 H), 0.47-0.66 (m, 2 H), 0.28-0.45 (m, 2 H)  −31.66 (c = 0.47, DCM) 18 Preparative HPLC (Method 2) 234

Free Base 744.4  3.59 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.69-7.89 (m, 4 H), 7.19 (d, 1 H), 7.12 (d, 1 H), 7.00 (dd, 1 H), 7.09 (t, 1 H), 5.93 (dd, 1 H), 4.39 (dd, 1 H), 3.85- 4.01 (m, 2 H), 3.72-3.85 (m, 1 H), 3.52-3.71 (m, 1 H), 3.45 (dd, 1 H), 3.17-3.27 (m, 2 H), 3.08 (dd, 1 H), 3.02 (br. s., 3 H), 2.93-2.99 (m, 1 H), 2.90 (br. s., 3 H), 2.75-2.85 (m, 1 H), 1.09-1.38 (m, 1 H), 0.48-0.66 (m, 2 H), 0.28-0.43 (m, 2 H)  −28.12 (c = 0.51, DCM) 18 Flash chromatography on silca gel 235

Free Base 671.34  4.09 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.76-7.86 (m, 2 H), 7.69-7.76 (m, 1 H), 7.57- 7.69 (m, 2 H), 7.19 (d, 1 H), 7.10 (d, 1 H), 6.98 (dd, 1 H), 7.07 (t, 1 H), 5.99 (dd, 1 H), 3.92 (dd, 1 H), 3.88 (dd, 1 H), 3.72-3.80 (m, 1 H), 3.47 (dd, 1 H), 3.28-3.37 (m, 1 H), 3.24 (dd, 1 H), 3.04-3.16 (m, 1 H), 2.83 (dd, 1 H), 2.55 (dd, 1 H), 1.62-1.91 (m, 1 H), 1.43-1.62 (m, 1 H), 1.29-1.45 (m, 2 H), 1.09- 1.29 (m, 1 H), 0.44-0.67 (m, 2 H), 0.21-0.43 (m, 2 H)  −79 (c = 0.23 DCM) 19 Preparative HPLC (Method 2) 236

Free Base 742.43  3.74 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.85 (dt, 1 H), 7.65-7.80 (m, 3 H), 7.19 (d, 1 H), 7.10 (d, 1 H), 6.98 (dd, 1 H), 7.07 (t, 1 H), 5.98 (dd, 1 H), 3.92 (dd, 1 H), 3.88 (dd, 1 H), 3.70-3.84 (m, 1 H), 3.46-3.54 (m, 2 H), 3.28-3.37 (m, 2 H), 3.24 (dd, 1 H), 3.07-3.19 (m, 1 H), 3.00 (br. s., 3 H), 2.88 (br. s., 3 H), 2.83 (dd, 1 H), 2.54- 2.65 (m, 1 H), 1.63-1.91 (m, 0 H), 1.48-1.63 (m, 0 H), 1.29-1.48 (m, 2 H), 1.05-1.29 (m, 1 H), 0.46-0.62 (m, 2 H), 0.17-0.46 (m, 2 H) 19 Preparative HPLC (Method 2) 237

Free Base 685.41  4.11 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.34-7.46 (m, 5 H), 7.19 (d, 1 H), 7.07 (d, 1 H), 6.93 (dd, 1 H), 7.07 (t, 1 H), 5.95 (dd, 1 H), 4.42 (s, 2 H), 3.91 (d, 2 H), 3.76-3.88 (m, 1 H), 3.35-3.43 (m, 2 H), 3.07-3.30 (m, 2 H), 2.61 (dd, 1 H), 2.34 (dd, 1 H), 1.64- 1.99 (m, 3 H), 1.27-1.49 (m, 1 H), 1.09-1.28 (m, 1 H), 0.48-0.67 (m, 2 H), 0.24-0.43 (m, 2 H)  −23.8 (c = 0.18, DCM) 19 Preparative HPLC (Method 2) followed by chromatograohy on silica gel 238

Free Base 764.1  4.06 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 8.10 (m, 2 H), 8.01 (m, 1 H), 7.93 (m, 1 H), 7.15- 7.21 (m, 1 H), 7.13 (m, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.94-7.03 (m, 1 H), 5.95-6.08 (m, 1 H), 4.18-4.28 (m, 1 H), 3.92 (d, J = 7.06 Hz, 2 H), 3.43-3.55 (m, 1 H), 3.36-3.43 (m, 1 H), 3.25-3.30 (m, 1 H), 3.16-3.23 (m, 1 H), 2.67 (s, 6 H), 1.94-2.05 (m, 1 H), 1.54- 1.79 (m, 3 H), 1.14-1.29 (m, 1 H), 0.48-0.63 (m, 2 H), 0.33 (d, J = 4.85 Hz, 2 H). 239

hydro- chloride 731.1  4.10 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 9.14 (d, J = 2.20 Hz, 1 H), 9.06 (d, J = 2.21 Hz, 1 H), 8.59 (s, 2 H), 7.16 (m, 1 H), 7.05-7.13 (m, 2 H), 6.92-6.99 (m, 1 H), 5.95- 6.10 (m, 1 H), 5.78 (s, 1 H), 3.82- 3.98 (m, 3 H), 3.65-3.79 (m, 1 H), 3.41-3.55 (m, 1 H), 3.34-3.38 (m, 1 H), 2.90-3.01 (m, 1 H), 2.67 (m, 4 H), 1.14-1.27 (m, 1 H), 0.56 (d, J = 7.94 Hz, 2 H), 0.33 (d, J = 4.85 Hz, 2 H). 240

hydro- chloride 744.2  4.07 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.93-8.97 (m, 1 H), 8.85- 8.90 (m, 1 H), 8.58 (s, 2 H), 7.14- 7.19 (m, 1 H), 7.05-7.12 (m, 2 H), 6.91-6.97 (m, 1 H), 5.96-6.04 (m, 1 H), 5.70 (s, 1 H), 4.03 (s, 3 H), 3.80-3.97 (m, 4 H), 3.60-3.76 (m, 1 H), 3.39-3.53 (m, 1 H), 3.23- 3.27 (m, 1 H), 2.88-2.98 (m, 1 H), 2.58 (m, 4 H), 1.12-1.33 (m, 1 H), 0.47-0.62 (m, 2 H), 0.20-0.41 (m, 2 H). 241

Free Base 735.2  3.47 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 12.45-12.98 (bs, 1 H), 8.59 (s, 2 H), 8.27 (d, J = 4.85 Hz, 1 H), 7.67 (d, J = 1.76 Hz, 1 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.06- 7.13 (m, 3 H), 6.96 (dd, J = 8.38, 1.76 Hz, 1 H), 6.03 (dd, J = 9.26, 4.85 Hz, 1 H), 5.22 (s, 1 H), 3.84- 3.96 (m, 5 H), 3.58-3.73 (m, 2 H), 3.45 (dd, J = 14.11, 9.26 Hz, 1 H), 3.28-3.30 (m, 1 H), 2.94-3.05 (m, 1 H), 2.75-2.84 (m, 1 H), 2.72 (d, J = 4.41 Hz, 3 H), 1.22 (d, J = 7.50 Hz, 1 H), 0.48-0.63 (m, 2 H), 0.33 (q, J = 4.85 Hz, 2 H) 242

Free Base 761.2  3.61 >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 12.46 (bs, 1 H), 8.57 (s, 2 H), 7.54 (dd, J = 3.53, 1.32 Hz, 1 H), 7.17 (d, J = 8.38 Hz, 1 H), 7.10 (d, J = 1.76 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.92-7.00 (m, 2 H), 6.01 (dd, J = 9.04, 5.07 Hz, 1 H), 5.46 (s, 1 H), 3.90 (dd, J = 7.06, 1.32 Hz, 2 H), 3.81 (ddd, J = 11.69, 6.17, 5.95 Hz, 1 H), 3.72 (t, J = 6.84 Hz, 2 H), 3.56-3.66 (m, 1 H), 3.39-3.55 (m, 3 H), 3.29 (d, J = 5.29 Hz, 1 H), 2.88-2.99 (m, 1 H), 2.64 (ddd, J = 10.81, 6.62, 6.39 Hz, 1 H), 1.91-2.02 (m, 2 H), 1.84 (q, J = 6.62 Hz, 2 H), 1.21 (ddd, J = 7.83, 4.52, 3.09 Hz, 1 H), 0.49-0.62 (m, 2 H), 0.28-0.40 (m, 2 H). 243

Free Base 663.2  4.62 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.59 (s, 2 H), 7.52 (m, 1 H), 7.17 (m, 1 H), 7.08-7.12 (m, 2 H), 7.07 (t, J = 75.00 Hz, 1 H), 6.95 (m, 1 H), 6.02-6.10 (m, 1 H), 5.46 (s, 1 H), 3.77-3.95 (m, 6 H), 3.65- 3.75 (m, 1 H), 3.47-3.59 (m, 1 H), 3.33-3.41 (m, 1 H), 2.96 (d, J = 15.88 Hz, 2H), 1.09-1.30 (m, 1 H), 0.46-0.62 (m, 2 H), 0.21-0.39 (m, 2 H). 328

Free Base 666.1  3.07; 3.11 (2)   21:79 244

Free Base 657.2  4.03; (3)   97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.74-7.83 (m, 2 H), 7.66-7.74 (m, 1 H), 7.57- 7.65 (m, 2 H), 7.21 (d, J = 8.38 Hz, 1 H), 7.14 (d, J = 1.76 Hz, 1 H), 7.09 (t, J = 75.00 Hz, 1 H), 7.00 (dd, J = 8.38, 1.76 Hz, 1 H), 5.98 (dd, J = 9.48, 4.63 Hz, 1 H), 4.14 (dd, J = 8.60, 4.63 Hz, 1 H), 3.86-4.01 (m, 2 H), 3.37-3.50 (m, 2 H), 3.27 (dd, J = 14.11, 4.41 Hz, 1 H), 3.14 (ddd, J = 9.81, 7.06, 6.95 Hz, 1 H), 1.45-1.98 (m, 4 H), 1.14-1.30 (m, 1 H), 0.48-0.63 (m, 2 H), 0.25-0.39 (m, 2 H). 245

Free Base 728.2  3.52 (2)    1:99 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.65-7.87 (m, 4 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.14 (d, J = 1.76 Hz, 1 H), 7.07 (t, J = 75.00 Hz, 1 H), 6.99 (m, 1 H), 5.96-6.08 (m, 1 H), 4.11-4.24 (m, 1 H), 3.91 (d, J = 7.06 Hz, 2 H), 3.33-3.51 (m, 2 H), 3.28 (m, 2 H), 2.83-3.06 (m, 6 H), 1.88-2.04 (m, 1 H), 1.45-1.76 (m, 3 H), 1.12- 1.29 (m, 1 H), 0.55 (dd, J = 8.16, 1.54 Hz, 2 H), 0.25-0.38 (m, 2 H). 246

Free Base 728.2  3.47 (2)   98:2 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.65-7.87 (m, 4 H), 7.18 (d, J = 7.94 Hz, 1H), 7.14 (d, J = 1.76 Hz, 1 H), 7.07 (t, J = 75.00 Hz, 1 H), 6.99 (m, 1 H), 5.96-6.08 (m, 1 H), 4.11-4.24 (m, 1 H), 3.91 (d, J = 7.06 Hz, 2 H), 3.33-3.51 (m, 2 H), 3.28 (m, 2 H), 2.83-3.06 (m, 6 H), 1.88-2.04 (m, 1 H), 1.45-1.76 (m, 3 H), 1.12- 1.29 (m, 1 H), 0.55 (dd, J = 8.16, 1.54 Hz, 2 H), 0.25-0.38 (m, 2 H). 247

Free Base 730.2   65:35 (¹H NMR) 248

Free Base 746.0  3.63 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.86-8.00 (m, 2 H), 7.65-7.83 (m, 2 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.11 (d, J = 1.32 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.86-6.96 (m, 1 H), 6.01 (dd, J = 9.04, 5.07 Hz, 1 H), 5.54 (s, 1 H), 3.80-3.98 (m, 3 H), 3.60-3.72 (m, 1 H), 3.46 (dd, J = 14.11, 9.26 Hz, 1 H), 3.30-3.35 (m, 1 H), 2.82-3.06 (m, 7 H), 2.63-2.73 (m, 1 H), 1.15-1.33 (m, 1 H), 0.47- 0.65 (m, 2 H), 0.33 (q, J = 4.85 Hz, 2 H) 249

Free Base 746.0  3.57; 3.64 (2)   84:16 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.89-7.98 (m, 2 H), 7.63-7.80 (m, 2 H), 7.22 (d, J = 7.94 Hz, 1 H), 7.06-7.15 (m, 2 H), 7.00 (dd, J = 8.38, 1.32 Hz, 1 H), 5.97 (dd, J = 9.70, 4.41 Hz, 1 H), 5.57 (s, 1 H), 3.89-4.02 (m, 2 H), 3.57-3.86 (m, 2 H), 3.47 (dd, J = 14.11, 9.70 Hz, 1 H), 3.26 (d, J = 4.85 Hz, 1 H), 2.80-3.10 (m, 7 H), 2.61-2.74 (m, 1 H), 1.15-1.31 (m, 1 H), 0.50-0.64 (m, 2 H), 0.34 (q, J = 4.85 Hz, 2 H) 250

Free Base 728.1  4.26 (2)    3:97 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.48 (s, 2 H), 7.12-7.21 (m, 2 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.95-7.02 (m, 2 H), 6.93 (d, J = 2.21 Hz, 1 H), 6.86 (d, J = 8.38 Hz, 1 H), 6.03 (dd, J = 9.70, 4.41 Hz, 1 H), 4.22-4.40 (m, 2 H), 4.11 (dd, J = 8.82, 3.97 Hz, 1 H), 3.92 (d, J = 7.06 Hz, 2 H), 3.45 (dd, J = 14.11, 9.70 Hz, 1 H), 3.08-3.27 (m, 5 H), 2.90 (s, 3 H), 1.83-2.01 (m, 1 H), 1.45-1.74 (m, 3 H), 1.13- 1.28 (m, 1 H), 0.48-0.65 (m, 2 H), 0.33 (q, J = 4.85 Hz, 2 H). 251

Free Base 713.1  4.00 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.92-9.04 (m, 1 H), 8.86- 8.92 (m, 1 H), 8.61 (s, 2 H), 7.12- 7.23 (m, 2 H), 7.07 (t, J = 75.00 Hz, 1 H), 6.95-7.02 (m, 1 H), 5.97-6.09 (m, 1 H), 4.34-4.41 (m, 1 H), 3.85-3.96 (m, 2 H), 3.38- 3.55 (m, 2 H), 3.19-3.29 (m, 2 H), 2.67 (s, 3 H), 1.89-2.06 (m, 1 H), 1.52-1.77 (m, 3 H), 1.10-1.31 (m, 1 H), 0.47-0.62 (m, 2 H), 0.27- 0.41 (m, 2 H). 252

Free Base 746.1  4.35 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.13-7.22 (m, 2 H), 6.94-7.10 (m, 4 H), 6.85 (d, J = 7.94 Hz, 1 H), 5.96-6.06 (m, 1 H), 4.85 (m, 1 H), (4.63 (d, J = 10.14 Hz, 1 H), 4.23-4.38 (m, 3 H), 3.92 (d, J = 7.06 Hz, 2 H), 3.40-3.52 (m, 1 H), 3.28 (m, 3 H), 2.96-3.08 (m, 1 H), 2.90 (m, 4 H), 1.13-1.29 (m, 1 H), 0.56 (dd, J = 8.38, 1.76 Hz, 2 H), 0.33 (d, J = 4.41 Hz, 2 H). 253

Free Base 731.0  4.08 (2) >99:1 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 9.13 (d, J = 2.21 Hz, 1 H), 9.02 (d, J = 2.21 Hz, 1 H), 8.59 (s, 2 H), 7.14-7.22 (m, 2 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.94-7.02 (m, 1 H), 5.93-6.10 (m, 1 H), 4.95- 5.09 (m, 1 H), 4.73-4.86 (m, 1 H), 4.27-4.44 (m, 1 H), 3.82-4.01 (m, 2 H), 3.41-3.55 (m, 1 H), 3.22- 3.28 (m, 1 H), 2.96-3.10 (m, 2 H), 2.66 (s, 3 H), 1.12-1.30 (m, 1 H), 0.50-0.64 (m, 2 H), 0.22-0.42 (m, 2 H). 254

Free Base 731.9  3.52 (2)    2:98 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.77 (d, J = 4.41 Hz, 1 H), 8.60 (s, 2 H), 8.30 (m, 1 H), 8.13- 8.22 (m, 1 H), 8.02 (d, J = 7.94 Hz, 1 H), 7.76 (t, J = 7.94 Hz, 1 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.11 (d, J = 1.32 Hz, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.95 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 8.82, 4.85 Hz, 1 H), 5.51 (s, 1 H), 3.87-3.97 (m, 2 H), 3.82 (ddd, J = 11.58, 5.95, 5.84 Hz, 1 H), 3.68 (ddd, J = 11.80, 6.39, 6.06 Hz, 1 H), 3.46 (dd, J = 14.11, 9.26 Hz, 1 H), 3.35 (m, 1 H), 2.90-3.03 (m, 1 H), 2.56-2.70 (m, 1 H), 1.13-1.31 (m, 1 H), 0.50-0.64 (m, 2 H), 0.27- 0.43 (m, 2 H).

Some of the compounds described above in Table 6 were further crystallized under the conditions described below in Table 7 to obtain one or more crystalline forms. Where reference in Table 7 is made to crystallization conditions (A), (B), (C), (D), or (E), the following operating conditions were used:

Temperature Cycling Experiments—(A)

Slurries of the materials were prepared in each of the selected solvent systems. Approximately 10 mg of material was slurried in ca. 200 μl of solvent (if material dissolved the clear solution was used). The slurries were temperature cycled at 40° C. in 4 hour cycles for a period of 3 days (the cooling/heating rates after the 4 hour periods were up was ca. 1° C./minute). Any solids present were isolated and allowed to dry at ambient conditions prior to analysis.

Slow Cooling Experiments—(B)

This was carried out by placing saturated solutions of the material in each of the selected solvent systems in an environment of 2° C. for ca. 3 days. A saturated solution was created and this exposed to the relevant experimental condition. Any solid material was then recovered and allowed to dry at ambient conditions prior to analysis.

Rapid Cooling Experiments—(C)

This was carried out by placing saturated solutions of the material, in each of the selected solvent systems in environment of −18° C. for ca. 3 days. A saturated solution was created and this exposed to the relevant experimental condition. Any solid material was then recovered and allowed to dry at ambient conditions prior to analysis.

Evaporation Experiments—(D)

Evaporation experiments were conducted on saturated mixtures as above described. This was carried out by allowing the solvents to evaporate freely at ambient conditions. Any solid material was then recovered and analysed after the solvent had evaporated to dryness.

Anti-Solvent Addition Experiments—(E)

Anti-solvent addition experiments were conducted on saturated solutions of the material in each of the respective solvent systems and adding anti-solvent until precipitation occurred. Any solid material was then recovered and allowed to dry at ambient conditions prior to analysis.

TABLE 7 Crystallization Entry Structure Solvent systems conditions Crystalline Form  52a

EtOH RT; 7.5 vv w/w I  52a

AcOEt/Heptane from 60 degrees to RT; 15 vv/12.5 vv w/w I  52a

IprOAc from RT to −20 degrees; 5 vv w/w I  52a

MeOH from 40 degrees to RT; 4 vv w/w I  52a

nBuOH; IprOH; Toluene; MTBE; (Ipr)₂O; EtOH (A) or (B) or (C) or (D) I  90a

MeOH From 50 degrees to RT; 10 vv v/w N/A  90b

nBuOH; MeoH; EtOH (A) or (B) or (C) or (D) I  90b

Dioxane; MIK (C) or (D) I  90b

Acetone; MEK (D) I  90c

(Ipr)₂O; IprOH; MTBE; Toluene (A) or (B) or (C) or (D) II  88a

Acetone (Ipr)₂O (A) I  88b

EtOH; Methyl Isobutyl Ketone (A) or (B) (with MIK) or (C) (with MIK) III  88c

MeOH (A) or (B) or (C) II  89a

n-BuOH; (Ipr)₂O ; IprOH; MTBE; (A) or (B) or (C) or (D) I  89b

EtOH; MeOH (A) or (B) or (C) or (D) II  93a

EtOH; MeOH; IprOH (A) or (B) or (C) or (D) I  93a

Acetone (D) I  93b

n-BuOH (B) or (C) or (D) II  91a

Acetone/MeOH From 50 degrees to RT; From 5/5 to 100% MeOH (acetone was evaporated) I  54a

EtOH From 50 degrees to RT; 5 vv v/w I 110a

MeOH RT, 5 vv v/w I 150a

EtOH (A) or (B) or (C) or (D) II 150b

nBuOH; MeOH (B) or (C) or (D) I  84a

EtOH (anti-solvent Cyclohexane) (A) or (B) or (C) or (D) or (E) I  84b

IprOH (anti- solvent Cyclohexane) (A) or (B) or (C) or (D) or (E) II  84b

nBuOH (anti- solvent Cyclohexane) (B) or (C) or (D) or (E) II  84c

(Ipr)₂O (anti- solvent Cyclohexane) (B) or (C) or (D) or (E) III 131a

nBuOH (anti- solvent Diisopropyl Ether) (C) or (D) or (E) I  97a

DCM; (Ipr)₂O; MTBE; Toluene; (A) I  97b

nBuOH; EtOH; Ethyl Acetate; MeOH; MEK; MIK; IprOH (A) II  97a

nBuOH; (Ipr)₂O; EtOH; IprOH; MTBE (B) or (C) I  97b

CH3CN; EtOAc; MeOH;MIK; Toluene (B) or (C) II 109a

Acetone; nBuOH; EtOH; Ethyl Acetate; MeOH; MIK; IprOH; Toluene Temperature Cycling (or Slow Cooling, except for MeOH, IprOH and Acetone) II 109b

MeOH; IprOH; (B) I 109c

(Ipr)₂O; MTBE (A) or (B) III

Example 9 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (123)

Step 1: 4-((2S)-2-(3-(3-carboxy-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide, (122)

3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (5) (60 mg, 0.112 mmol) was dissolved in pyridine (1 ml), then 5-(chlorosulfonyl)-2-methoxybenzoic acid (56 ml, 0.224 mmol) was added at 0° C., and the mixture was stirred at RT for 2 hours. The reaction was quenched with HCl 1N, and the product was extracted with AcOEt. The organic phase was washed with HCl 1N (×2) and brine, then dried over Na₂SO₄. The solvent was removed to yield 70 mg of the desired compound (yield 83%). MS/ESI⁺ 749.0 [MH]⁺; t_(R)=5.94; 6.02 (Method 1); Diastereomeric Ratio=32:68.

Step 2: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (123)

4-((2S)-2-(3-(3-carboxy-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (122) (70 mg, 0.093 mmol) was dissolved in DMF (1 ml). CDI (18 mg, 0.112 mmol) was added, and the mixture stirred for 30 minutes at RT. Then dimethylamine 2M in THF was added (3000, 0.600 mmol), and the mixture stirred at RT for 2 hours. The reaction was quenched with water, and the product was extracted with AcOEt. The organic layer was washed with water (2×) and NaCl saturated solution, dried over Na₂SO₄ and evaporated under vacuum. The crude product was purified by preparative HPLC (Method 1) condition to give 70 mg of the desired compound (yield 97%). MS/ESI⁺ 776.1 [MH]⁺; t_(R) (Method 1)=6.40; 6.50 min; Diasteromeric Ratio=36:64.

The compounds listed in Table 8 were prepared according to analogous procedure as that described for Scheme 17 and by reacting the appropriate precursors listed with suitable reagents, followed by an appropriate purification procedure as below indicated.

TABLE 8 HPLC-MS characterization t_(R)/min Methods Diastereomeric Purification Entry Structure SALT NAME MS/ESI⁺ [MH]⁺ 1 or 2 ratio ¹H NMR [α]_(D) Precursor Method Amine 124

Free Base 757.09 3.56 (2) >99:1  ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.80 (dd, J = 8.60, 2.43 Hz, 1 H), 7.56 (d, J = 2.65 Hz, 1 H), 7.32 (d, J = 8.82 Hz, 1 H), 7.10- 7.21 (m, 2 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.98 (dd, J = 8.38, 1.76 Hz, 1 H), 5.89- 6.11 (m, 1 H), 4.04- 4.20 (m, 1 H), 3.87- 3.97 (m, 5 H), 3.46 (m, 1 H), 3.08-3.30 (m, 3 H), 2.99 (s, 3 H), 2.75 (s, 3 H), 1.60-1.75 (m, 2 H), 1.43-1.59 (m, 2 H), 0.85 (m, 1 H), 0.49- 0.62 (m, 2 H), 0.33 (d, J = 4.41 Hz, 2 H). −55.88 (c = 0.48; CHCl₃) 3 Preparative HPLC (Method 1)

125

Free Base 747.0 6.37; 6.47 (1) 38:62 5 Preparative HPLC (Method 1)

126

formate 801.1 4.78; 4.88 (1) 38:62 5 Preparative HPLC (Method 1)

127

Free Base 831.1 4.85; 4.92 (2) 26:74 5 No purification

128

Free Base 818.0 6.32; 6.40 (2) 33:67 5 No purification

129

Free Base 772.3 3.84 (2) >99:1  ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.62 (s, 2 H), 7.59- 7.77 (m, 1 H), 7.45- 7.56 (m, 1 H), 7.18- 7.22 (m, 1 H), 7.13- 7.17 (m, 1 H), 7.03- 7.09 (m, 2 H), 6.79- 6.95 (m, 1 H), 5.83- 5.94 (m, 1 H), 4.53- 4.72 (m, 1 H), 3.81- 3.96 (m, 5 H), 3.60 (d, J = 11.91 Hz, 1 H), 3.40 (d, J = 10.58 Hz, 1 H), 3.28-3.29 (m, 1 H), 3.23 (dd, J = 14.11, 5.29 Hz, 1 H), 2.98 (s, 3 H), 2.74 (s, 3 H), 2.06 (d, J = 12.79 Hz, 1 H), 1.43-1.61 (m, 3 H), 1.12-1.31 (m, 2 H), 0.88 (d, J = 12.79 Hz, 1 H), 0.52-0.61 (m, 2 H), 0.29-0.36 (m, 2 H). 10  Preparative HPLC (Method 1)

130

formate 801.2 2.59; 2.64 (2) 29:71 5 Triturated with Et₂O

131

Free Base 776.2 3.64 (2) 97:3  ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.81- 7.97 (m, 1 H), 7.68- 7.76 (m, 1 H), 7.32 (m, 1 H), 7.18 (d, J = 7.94 Hz, 1 H), 7.05- 7.13 (m, 2 H), 6.91- 6.98 (m, 1 H), 5.92- 6.07 (m, 1 H), 5.57- (s, 1 H), 3.75-4.06 (m, 6 H), 3.55-3.68 (m, 1 H), 3.37-3.49 (m, 1 H), 3.25-3.35 (m, 1 H), 2.99 (s, 4 H), 2.75 (s, 3 H), 2.54-2.65 (m, 1 H), 1.14-1.29 (m, 1 H), 0.56 (dd, J = 7.94, 1.76 Hz, 2 H), 0.33 (d, J = 5.29 Hz, 2 H). 6 Preparative HPLC (Method 1)

132

Free Base 801.2 2.66 (2) >99:1  ¹H NMR (400 MHz, DMSO-d₆) δ ppm 9.66-9.90 (bs, 1 H), 8.58 (s, 2 H), 7.95 (m, 2 H), 7.65-7.86 (m, 2 H), 7.19 (d, J = 8.38 Hz, 1 H), 7.10 (d, J = 9.26 Hz, 2 H), 6.97 (m, 1 H), 5.94- 6.12 (m, 1 H), 5.53 (s, 1 H), 3.90 (m, 3 H), 3.60-3.77 (m, 2 H), 3.38 (m, 3 H), 3.25-3.30 (m, 3 H), 2.93-3.22 (m, 4 H), 2.81 (s, 3 H), 2.55- 2.73 (m, 1 H), 2.29 (s, 3 H), 1.16-1.30 (m, 1 H), 0.57 (d, J = 7.94 Hz, 2 H), 0.33 (d, J = 4.41 Hz, 2 H). 6 Preparative HPLC (Method 1)

The compound listed in Table 9 was prepared under analogous conditions to those described in Scheme 17 by reacting the appropriate precursor listed with suitable reagents and using an alcohol nucleofile in step 2 in place of an amine, followed by a purification step as below indicated.

TABLE 9 HPLC-MS characterization MS/ t_(R)/min Diastereo- Pur- SALT ESI⁺ Methods meric Pre- ification Entry Structure NAME [MH]⁺ 1 or 2 ratio ¹H NMR cursor Method Alcohol 133

for- mate 832.1 3.12 (2) 97:3 ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 8.23-8.35 (m, 2 H), 8.12-8.20 (m, 1 H), 7.84 (t, J = 7.94 Hz, 1 H), 7.18 (d, J = 8.38 Hz, 1 H), 7.05- 7.15 (m, 2 H), 6.95 (dd, J = 8.38, 1.76 Hz, 1 H), 6.01 (dd, J = 9.04, 5.07 Hz, 1 H), 5.48 (s, 1 H), 4.45 (t, J = 5.51 Hz, 2 H), 3.89 (d, J = 6.62 Hz, 2 H), 3.74- 3.82 (m, 1 H), 3.64-3.72 (m, 1 H), 3.50-3.60 (m, 4 H), 3.46 (dd, J = 14.11, 9.26 Hz, 1 H), 3.30 (dd, J = 14.11, 4.85 Hz, 1 H), 2.94-3.04 (m, 1 H), 2.66- 2.78 (m, 3 H), 2.47 (d, J = 4.41 Hz, 4 H), 1.15- 1.28 (m, 1 H), 0.51-0.60 (m, 2 H), 0.28-0.38 (m, 2H). 5 No pur- ification

Example 10 Synthesis of 4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (135)

Step 1: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-nitrophenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (134)

3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (1.2 g, 2.24 mmol) was dissolved in pyridine (6 ml), then 4-nitrobenzene-1-sulfonyl chloride (596 mg, 2.69 mmol) was added at 0° C., and the mixture was stirred at RT for 2 hours. The reaction was quenched with HCl 1N, and the product was extracted with AcOEt. The organic phase was washed with HCl 1N (×2) and brine, then dried over Na₂SO₄. The solvent was removed to yield 1.5 g of the desired compound (yield 93%). MS/ESI⁺ 720.04 [MH]⁺

Step 2: 4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (135) 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-nitrophenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (134) (1 g, 1.388 mmol), was dissolved in THF (10 ml). Tin(II) chloride dihydrate (3.13 g, 13.881 mmol) was added, and the mixture was stirred at RT for 2 days. The solvent was removed under vacuum, and the crude product was dissolved in AcOEt and diluted with HCl 1N. Diatomaceus earth was added to the emulsion, and the mixture was filtered on a Diatomaceus earth pad. The organic phase was washed with HCl 1N, brine, dried over Na₂SO₄ and concentrated under vacuum to give 1.5 g of crude, that was purified by Flash Chromatography (DCM/IPA 97:3) to obtain 780 mg of the final compound (1.130 mmol, yield 81%). MS/ESI⁺ 689.9 [MH]⁺; t_(R)=6.30; 6.40 (Method 1); Diastereomeric Ratio=38:62

The compounds listed in Table 10 were prepared according to analogous procedures as those described for Scheme 11 and by reacting the corresponding precursors listed with suitable reagents, followed by a purification step as below indicated.

TABLE 10 HPLC-MS characterization t_(R)/min Methods Diastereomeric Purification Sulfonyl Entry Structure SALT NAME MS/ESI⁺ [MH]⁺ 1 or 2 ratio ¹H NMR [α]_(D) Precursor Method chloride 136

Free Base 671.9 6.14 (1) >99:1  ¹H NMR (400 MHz, DMSO- d₆) δ ppm 8.59 (s, 2 H), 7.35- 7.44 (m, 2 H),7.12-7.22 (m, 2 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.95-7.02 (m, 1 H), 6.53-6.71 (m, 2 H), 6.06-6.17 (bs, 2 H),5.95- 6.04 (m, 1 H), 3.95-4.01 (m, 1 H), 3.86- 3.94 (m, 2 H), 3.43-3.53 (m, 1 H), 3.21- 3.30 (m, 3 H), 2.99-3.13 (m,1 H), 1.83- 1.95 (m, 1 H), 1.55-1.68 (m, 2 H), 1.35- 1.54 (m, 1 H), 1.18-1.29 (m, 1 H), 0.49- 0.63 (m, 2 H), 0.26-0.39 (m, 2 H). 3 Crystallization from AcOEt/Hexane

137

Free Base 719.8 6.67; 6.79 (1) 41:59 +88.93 (c = 0.51; CHCl₃) 5 Preparative HPLC (Method 1)

138

Free Base 690.0 6.34 (1) >99:1  ¹H NMR (400 MHz, DMSO- d₆) δ ppm 8.57 (s, 2 H), 7.46 (d, J = 8.82 Hz, 2 H), 7.15-7.20 (m, 1 H), 7.11- 7.15 (m, 1 H), 7.08 (t, J = 75.00 Hz, 1 H), 6.93- 6.99 (m, 1 H), 6.62 (d, J = 8.38 Hz, 2 H), 6.15 (s, 2 H), 5.96- 6.05 (m, 1 H), 4.63-4.74 (m, 1 H), 4.50- 4.59 (m, 1 H), 4.19-4.27 (m, 1 H), 3.91 (d, J = 6.62 Hz, 2 H), 3.39-3.50 (m, 1 H), 3.21- 3.29 (m, 1 H), 2.93-3.02 (m, 1 H), 2.82- 2.90 (m, 1 H), 1.16-1.27 (m, 1 H), 0.51- 0.61 (m, 2 H), 0.28-0.39 (m, 2 H). 11 Preparative HPLC (Method 1)

139

Free Base 688.0 5.80; 5.97 (1) 63:37 8 Preparative HPLC (Method 1)

140

Free Base 690.2 3.79 (2) 99:1  ¹H NMR (400 MHz, DMSO- d₆) δ ppm 8.59 (s, 2 H), 7.22- 7.30 (m, 1 H), 7.15-7.21 (m, 1 H), 7.08 (m, 2 H), 6.93-7.03 (m, 2 H), 6.80- 6.92 (m, 2 H), 5.92-6.07 (m, 1 H), 5.61- 5.74 (bs, 2 H), 5.25 (s, 1 H), 3.90 (d, J = 7.06 Hz, 2 H), 3.59- 3.79 (m, 2 H), 3.39-3.51 (m, 1 H), 3.14- 3.24 (m, 1 H), 2.90-3.05 (m, 1 H), 2.62- 2.75 (m, 1 H), 1.14-1.28 (m, 1 H), 0.51- 0.60 (m, 1 H), 0.27-0.41 (m, 1 H). 6 Preparative HPLC (Method 1)

141

Free Base 701.3 ¹H NMR (400 MHz, DMSO- d₆)  

  ppm 8.56 (s, 2 H), 7.32 (d, J = 8.82 Hz, 2 H), 7.14-7.20 (m, 1 H), 7.06 (m, 2 H), 6.91- 6.98 (m, 1 H), 6.64 (d, J = 8.82 Hz, 2 H), 6.08 (bs, 2 H), 5.93- 6.03 (m, 1 H), 3.79-4.05 (m, 2 H), 3.37- 3.58 (m, 2 H), 3.21 (dd, J = 13.89, 4.63 Hz, 2 H), 2.68- 2.83 (m, 4 H), 2.40-2.48 (m, 4 H), 1.09- 1.28 (m, 1 H), 0.50-0.65 (m, 2 H), 0.23- 0.44 (m, 2 H). na 14 Preparative HPLC (Method 1)

Example 11 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(N-(2-morpholinoethyl)methylsulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide formate (143)

Step 1: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(methylsulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (142)

4-((2S)-2-(3-(4-aminophenyl sulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (135) (128 mg, 0.185 mmol), obtained according to analogous procedure as that described in Example 9, was dissolved in DCM (1.5 ml). Pyridine (29.3 mg, 0.371 mmol) and methanesulfonyl chloride (36.1 mg, 0.315 mmol) were added, and the reaction was stirred at RT for 3 hours to achieve completion. The reaction mixture was diluted with DCM and extracted with HCl 1N. The organic phase was washed with HCl 1N and brine, dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by preparative HPLC (Method 1) to give 80 mg of the final compound (yield 56%). MS/ESI⁺ 767.9 [MH]⁺, t_(R)=6.25; 6.35 min (Method 1); Diastereomeric Ratio: 40:60.

Step 2: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(N-(2-morpholinoethyl)methylsulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide formate (143)

3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(methyl sulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide, (142) (80 mg, 0.104 mmol) was dissolved in DMF (1.5 ml). 4-(2-chloroethyl)morpholine (78 mg, 0.520 mmol) and K₂CO₃ (17.26 mg, 0.125 mmol) were added, and the reaction is stirred at 45° C. for 6 hours to achieve completion. The reaction mixture was diluted with water and extracted with AcOEt. The organic phase was dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by preparative HPLC (Method 1) to give 40 mg of the final compound as formate salt (yield 44%).

MS/ESI⁺ 880.9 [MH]⁺; 5 t_(R)=5.15; 5.28 min (Method 1); Diastereomeric Ratio=37:63.

Example 12 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(2-oxo-2-(thiophen-2-yl)ethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine1-oxide (144)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (5) (70 mg, 0.131 mmol) was dissolved in DMF (1 ml). K₂CO₃ (22 mg, 0.157 mmol) and 2-bromo-1-(thiophen-2-yl)ethanone (80 mg, 0.392 mmol) were added, and the reaction is stirred at 45° C. for 3 hours to achieve completion. The reaction mixture was diluted with water and extracted with AcOEt. The organic phase was dried over Na₂SO₄ and concentrated under vacuum. The crude product was purified by preparative HPLC (Method 1) to give 50 mg of the final product, (yield 58%). MS/ESI⁺ 658.9 [MH]⁺; t_(R) (Method 2)=7.10; 7.24 min; Diastereomeric Ratio=44:56

The compounds listed in Table 16 were prepared according to analogous procedure as that described for Scheme 20 and by reacting the appropriate precursors listed (obtained as free base after basic treatment of hydrochloride salt with aqueous sat. NaHCO₃ followed by extraction with DCM) with suitable commercial reagents, using CH₃CN instead of DMF as the solvent and heating at 70° C., followed by an appropriate purification step as below indicated.

TABLE 16 HPLC-MS characterization MS/ t_(R)/min Diastere- ESI⁺ Method omeric Purification Alkylation Entry Structure SALT NAME [MH]⁺ 1, 2 or 3 ratio ¹H NMR [α]_(D) Precursor Method reagent 255

Free Base 653.19 4.21:4.28 (3)    5:95 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.54 (s, 2 H), 7.87-8.02 (m, 2 H), 7.61-7.71 (m, 1 H), 7.47-7.61 (m, 2 H), 7.18 (d, 1 H), 7.13 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 5.98 (dd, 1 H), 4.89 (s, 1H), 4.11 (d, 1 H), 3.99 (d, 1 H), 3.92 (d, 2 H), 3.41-3.56 (m, 2 H), 3.13-3.32 (m, 2 H), 2.83-3.08 (m, 2 H), 1.02-1.41 (m, 1 H), 0.50-0.65 (m, 2 H), 0.23-0.43 (m, 2 H) −38.6  (c = 0.62, DCM) Free Base of 6 Preparative HPLC (Method 2)

256

Free Base 635.28 3.16 (3) >95:5  (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.50 (s, 2 H), 7.82-8.01 (m, 2 H), 7.56-7.69 (m, 1 H), 7.41-7.56 (m, 2 H), 7.16 (d, 1 H), 7.07 (d, 1 H), 6.96 (dd, 1 H), 7.05 (t, 1 H), 5.99 (dd, 1 H), 4.18 (d, 1 H), 3.82-3.93 (m, 2 H), 3.86 (d, 1 H), 3.51 (dd, 1 H), 3.44 (dd, 1 H), 3.23 (dd, 1 H), 2.87-3.05 (m, 1 H), 2.54-2.69 (m, 1 H), 2.02-2.22 (m, 1 H), 1.52-1.89 (m, 3 H), 1.02-1.34 (m, 1 H), 0.44-0.64 (m, 2 H), 0.15-0.44 (m, 2 H) −52.52 (c = 0.23, MeOH) Free Base of 3 Flash chromatography on silica gel followed by trituration with iPr₂O

257

trifluoroacetate 607.28 3.02 (3) >95:5  (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 10.04 (br. s., 1 H), 8.59 (s, 2 H), 7.40 (br. s., 5 H), 7.19 (d, 1 H), 7.08 (d, l H), 6.95 (dd, 1 H), 7.07 (t, 1 H), 5.50-5.96 (m, 1 H), 4.08-4.68 (m, 3 H), 3.89 (d, 2 H), 3.42 (dd, 1 H), 3.26-3.37 (m, 2 H), 3.21 (dd, 1 H), 2.31-2.47 (m, 1 H), 1.96-2.17 (m, 1 H), 1.60-1.93 (m, 2 H), 1.12-1.31 (m, 1 H), 0.47-0.73 (m, 2 H), 0.23-0.45 (m, 2 H) −31.90 (c = 0.2, DCM) Free Base of 3 Flash chromatography on silica gel followed by preparative HPLC (Method 2)

258

hydrochloride 678.43 2.86 (3) >95:5  (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 10.30 (br. s., 1 H), 8.59 (s, 2 H), 7.37-7.60 (m, 4 H), 7.19 (d, 1 H), 7.09 (d, 1H), 6.94 (dd, 1 H), 7.07 (t, 1 H), 5.80 (br. s., 1 H), 4.22-4.68 (m, 3 H), 3.89 (d, 2 H), 3.44 (dd, 1 H), 3.27-3.38 (m, 1 H), 3.23 (dd, 1 H), 2.99 (br. s., 3 H), 2.92-2.98 (m, 1 H), 2.90 (br. s., 3 H), 2.56-2.68 (m, 1 H), 1.67-2.23 (m, 3 H), 1.14-1.35 (m, 1 H), 0.48-0.75 (m, 2 H), 0.24-0.44 (m, 2 H) −37.2  (c = 0.32, DCM) Free Base of 3 Preparative HLC (method 2) followed by dissolution in DCM, treatment with 4M HCl in dioxane, evaporation and trituration with Et₂O

Example 21 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)-2-oxoethyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (261)

Step 1: Acetyl-N,N-dimethylbenzamide (259)

3-Acetylbenzoic acid (400 mg, 2.437 mmol), dimethylamine hydrochloride (238 mg, 2.92 mmol), EDC (701 mg, 3.66 mmol), and DMAP (447 mg, 3.66 mmol) were dissolved in DCM (80 ml), and the resulting solution was stirred at RT overnight. The reaction mixture was washed twice with aqueous 1N HCl and with brine; the organic phase was dried over Na₂SO₄, filtered and evaporated to give the desired product (450 mg, 2.353 mmol, 97% yield); MS/ESI⁺ 192.12 [MH]⁺.

Step 2: 3-(2-bromoacetyl)-N,N-dimethylbenzamide (260)

To a solution of 3-acetyl-N,N-dimethylbenzamide (450 mg, 2.353 mmol) in DCM (20 ml), bromine (0.121 ml, 2.353 mmol) was added drop-wise. The resulting dark solution was stirred at RT for 24 hours. More bromine (60 ml, 1164 mmol) was added, and the stirring was continued for 4 hours. The solution was washed twice with aqueous sat. NaHCO₃ solution, and the organic layer was dried over Na₂SO₄. The solvent was removed under vacuum to afford the desired product (526 mg, 1.947 mmol, 83% yield), which was employed in the next step without further purification. MS/ESI⁺ 269.96 [MH]⁺.

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)-2-oxoethyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (261)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)-2-oxoethyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide was prepared according to analogous procedure as that described for Scheme 20 (Example 12) starting from intermediate (6), obtained as free base after basic treatment of the hydrochloride salt with aqueous sat. NaHCO₃ followed by extraction with DCM, usign CH₃CN as the solvent and heating at 60° C. It was purified by preparative HPLC (Method 2) (41% yield); MS/ESI⁺ 724.24 [MH]⁺; t_(R) (Method 3)=3.82 min; Diastereomeric Ratio >95:5 (¹H NMR); □□_(D)]=−40.6 (c=0.38, DCM).

¹H NMR (B) (300 MHz, DMSO-d6) 8 ppm 8.54 (s, 2H), 8.00 (dt, 1H), 7.96 (t, 1H), 7.67 (dt, 1H), 7.60 (t, 1H), 7.18 (d, 1H), 7.13 (d, 1H), 6.96 (dd, 1H), 6.81-7.41 (m, 1H), 5.98 (dd, 1H), 4.90 (s, 1H), 4.13 (d, 1H), 4.02 (d, 1H), 3.92 (d, 2H), 3.45-3.55 (m, 1H), 3.40 (dd, 1H), 3.28 (m, 0H), 3.13-3.23 (m, 1H), 3.01 (br. s., 3H), 2.86-2.94 (m, 4H), 2.82-3.05 (m, 2H), 1.07-1.39 (m, 1H), 0.45-0.70 (m, 2H), 0.18-0.44 (m, 2H)

The compound listed in Table 17 was prepared according to analogous procedures as those described for Scheme 28 and by reacting the appropriate precursor listed (obtained as free base after basic treatment of the hydrochloride salt with aqueous sat. NaHCO₃ followed by extraction with DCM), heating at 70° C. in Step 3, followed by an appropriate purification step as below indicated.

TABLE 17 HPLC-MS characterization Dia- MS/ t_(R)/min stereo- Purifi- SALT ESI⁺ Method meric Pre- cation Entry Structure NAME [MH]⁺ 1 or 2 ratio ¹H NMR [α]_(D) cursor Method 262

tri- fluoro- acetate 706.25 2.98 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO- d₆) δ ppm 8.56 (s, 2 H), 8.01 (dt, 1 H), 7.97 (t, 1 H), 7.77 (dt, 1 H), 7.66 (t, 1 H), 7.21 (d, 1 H), 7.14 (d, 1 H), 7.00 (dd, 1 H), 7.08 (t, 1 H), 6.08 (dd, 1 H), 5.00 (br. s., 2 H), 4.38 (br. s., 1 H), 3.91 (d, 2 H), 3.60 (br. s., 1 H), 3.53 (dd, 1 H), 3.30 (dd, 1 H), 3.19 (br. s., 1 H), 3.02 (br. s., 3 H), 2.92 (br. s., 3 H), 2.32- 2.46 (m, 1 H), 1.68-2.18 (m, 3 H), 1.05- 1.36 (m, 1 H), 0.51-0.72 (m, 2 H), 0.22- 0.40 (m, 2 H) −19.6 (c = 0.37, DCM). Free Base of 3 Prepar- ative HPLC (Meth- od 2)

Example 13 Synthesis of 4-((S)-2-((S)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (150)

Step 1: methyl 3-(4-nitrophenylsulfonyl)thiazolidine-2-carboxylate (146)

Methyl thiazolidine-2-carboxylate hydrochloride (145) (20 g; 109 mmol) was dissolved in pyridine (100 ml), then 4-nitrobenzene-1-sulfonyl chloride (27 g, 124 mmol) was added at 0° C., and the mixture was stirred for 3 hours. After that time, the reaction was quenched with HCl 1N to precipitate a solid that was filtered on a fit and washed with water several times. The orange solid was triturated in acetone, washed with acetone (×2) and dried under vacuum to yield 27 g (76%).

MS/ESI⁺ 333.01 [MH]⁺

Step 2: methyl 3-(4-aminophenylsulfonyl)thiazolidine-2-carboxylate hydrochloride (147)

A mixture of methyl 3-(4-nitrophenylsulfonyl)thiazolidine-2-carboxylate (146) (5.74 g; 17.27 mmol) and 5% Pd/C (16 g; 7.547 mmol) in 600 ml of MeOH and 400 ml of HCl 1N was hydrogenated for 10 hrs at 50 psi. After that time, the reaction was filtered over Celite, washed with MeOH and the solution was concentrated under vacuum to yield the desired product (10.47 g; 72%). MS/ESI⁺ 312.04 [MH]⁺

Step 3: 3-(4-aminophenylsulfonyl)thiazolidine-2-carboxylic acid (148)

To a solution of methyl 3-(4-aminophenylsulfonyl)thiazolidine-2-carboxylate hydrochloride (147) (7.43 g, 24.57 mmol) in MeOH (62 ml), LiOH 1M (62 ml) was added. The solution was stirred at room temperature for 1 hour, then the pH was adjusted to 6 with HCl 1M. MeOH was evaporated under reduced pressure, and HCl 1M was added until the pH=3 and the mixture cooled at 0 degrees for 3 hours, until complete precipitation. The solid was filtered, washed with water and dried in vacuo at 45 degrees to give 6.44 g of the desired product (yield 91%).

MS/ESI⁺ 289.02 [MH]⁺

Step 4: 4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (149)

To a solution of (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (1.55 g, 3.69 mmol) dissolved in DMF (20 ml), EDC (2.83 g, 14.77 mmol) and 3-(4-aminophenylsulfonyl)thiazolidine-2-carboxylic acid (148) (1.81 g, 6.28 mmol) were added. The mixture was cooled at 0 degrees, and DMAP (0.541 g. 4.43 mmol) was added. The mixture was stirred at −20 degrees for 20 minutes, then it was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was poured into water (500 ml), and the precipitate isolated by filtration. The filtered solid was washed with water (150 ml) and dried in vacuo at 45 degrees to afford 2.49 g of the desired product (yield 98%). MS/ESI⁺ 689.8 [MH]⁺

Step 5: 4-((S)-2-((S)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (150)

4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (149) (2.49 g, 3.61 mmol) was dissolved in EtOH (35 ml) at 50 degrees, and a solution of methansulfonic acid in EtOH 10% w/w was added (3.47 g, 3.61 mmol) to achieve salification. The methanesulfonate salt was filtered off and crystallized again from hot EtOH (25 ml). The salt was dissolved in CH₂Cl₂ (40 ml), and NaHCO₃ sat sol (30 ml) was added. The mixture was stirred for 30 minutes at RT, and then the two phases were separated. The organic phase was dried over Na₂SO₄ and evaporated under reduced pressure to afford a solid which was crystallized again from hot EtOH (25 ml) to yield 800 mg of the desired product. MS/ESI⁺ 689.8 [MH]⁺; t_(R) (Method 1)=6.37 min; [α_(D)]=+38.57 (c=0.49; CHCl₃). ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.58 (s, 2H), 7.42-7.52 (m, 2H), 7.14-7.20 (m, 1H), 7.05-7.12 (m, 2H), 6.90-6.97 (m, 1H), 6.60-6.69 (m, 2H), 6.15-6.24 (s, 2H), 5.96-6.05 (m, 1H), 5.29 (s, 1H), 3.86-3.95 (m, 2H), 3.68-3.80 (m, 1H), 3.52 (d, J=47.63 Hz, 1H), 3.38-3.48 (m, 1H), 3.29 (m, 1H), 2.84-2.99 (m, 1H), 2.53-2.60 (m, 1H), 1.22-1.36 (m, 1H), 0.46-0.63 (m, 2H), 0.28-0.40 (m, 2H).

The compound listed in Table 11 was prepared according to analogous procedures as those described for Scheme 21 (Steps 1-4), followed by purification of compound (131), through Flash Cromatography eluting with DCM/n-Hexane/i-PrOH/EtOH=55/40/4/1.

TABLE 11 HPLC-MS characterization t_(R)/min Diastere- SALT MS/ESI⁺ Methods omeric Entry Structure NAME [MH]⁺ 1 or 2 ratio ¹H NMR [α]_(D) 151

Free Base 689.8 6.28 (1) >99:1 ¹H NMR (400 MHz, DMSO-d₆) □ ppm 8.54 (s, 2 H), 7.44-7.50 (m, 2 H), 7.17-7.24 (m, 1 H), 7.07- 7.14 (m, 2 H), 6.94-7.03 (m, 1 H), 6.57-6.64 (m, 2 H), 6.18 (s, 2 H), 5.84-6.01 (m, 1 H), 5.27 (s, 1 H), 3.86-3.99 (m, 2 H), 3.55-3.72 (m, 2 H), 3.38- 3.51 (m, 1 H), 3.25 (m, 1 H), 2.94-3.06 (m, 1 H), 2.55-2.64 (m, 1 H), 1.24-1.31 (m, 1 H), 0.46- 0.67 (m, 2 H), 0.27-0.42 (m, 2 H) −41.36 (c = 0.51; CHCl₃)

Example 14 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (155)

Step 1: (S)-methyl 1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carboxylate (153)

(S)-methylpyrrolidine-2-carboxylate (152) (50 mg; 0.387 mmol) was dissolved in pyridine (1 ml), then 1-methyl-1H-imidazole-2-sulfonyl chloride (70 mg, 0.387 mmol) was added at 0° C., and the mixture was stirred for 3 hours. After that time, the reaction was quenched with HCl 1N and extracted with AcOEt twice. The organic phase was dried over Na₂SO₄ and evaporated under vacuum to yield 50 mg (yield 47%).

MS/ESI⁺ 274.08 [MH]⁺

Step 2: (S)-1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carboxylic acid (154)

A solution of (S)-methyl 1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carboxylate (153) (50 mg, 0.183 mmol) in HCl/Dioxane 4M (1 ml) was reacted under microwave irradiation at 100 degrees for 30 minutes. Then Dioxane was evaporated under reduced pressure to yield 40 mg of the desired compound (yield 84%).

MS/ESI⁺ 260.06 [MH]⁺

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (155)

To a solution of (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (20 mg, 0.048 mmol) dissolved in DMF (1 ml), EDC (9 mg, 0.048 mmol) and 3-(4-aminophenylsulfonyl)thiazolidine-2-carboxylic acid (154) (40 mg, 0.154 mmol) were added. The mixture was cooled at 0 degrees, and DMAP (6 mg. 0.048 mmol) was added. The mixture was stirred at −20 degrees for 20 minutes, and then it was allowed to warm to RT and stirred for 3 hours. The reaction mixture was poured into water and extracted with AcOEt (×3). The organic phase was dried over Na₂SO₄, evaporated in vacuo to afford 30 mg of the desired product (yield 95%). MS/ESI⁺ 661.3 [MH]⁺; t_(R) (Method 2)=3.60 min; Diastereomeric Ratio=99:1; ¹H NMR (400 MHz, DMSO-d₆) δ ppm 8.51 (s, 2 H), 7.47 (m, 1H), 7.18 (d, J=7.94 Hz, 1H), 7.13 (d, J=1.76 Hz, 1H), 7.08 (d, J=4.41 Hz, 2H), 6.98 (dd, J=8.38, 1.76 Hz, 1H), 6.00 (dd, J=9.48, 4.63 Hz, 1H), 4.47 (dd, J=8.82, 4.41 Hz, 1H), 3.92 (dd, J=7.06, 1.76 Hz, 2H), 3.84 (s, 3H), 3.37-3.55 (m, 3H), 3.24 (dd, J=14.11, 4.41 Hz, 1H), 2.22-2.37 (m, 1H), 1.83-1.95 (m, 1H), 1.65-1.82 (m, 2 H), 1.12-1.30 (m, 1H), 0.49-0.64 (m, 2H), 0.28-0.42 (m, 2H).

Example 22 Synthesis of 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (263)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (Compound 52) (200 mg, 0.268 mmol) was dissolved in 2,2,2-trifluoroacetic acid (2 ml, 0.268 mmol), and the solution stirred overnight at RT. The reaction mixture was diluted with DCM and concentrated under vacuum (2×) to give a crude which was purified through preparative HPLC (method 1) to give 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (90 mg, 0.130 mmol, 49% yield). MS/ESI⁺ 661.3 [MH]⁺; t_(R) (Method 2)=2.49; Diastereomeric Ratio=99:1; ¹H NMR (400 MHz, DMSO-d₆) δ ppm 10.05 (s, 1H), 8.58 (s, 2H), 7.85 7.97 (m, 2H), 7.67-7.80 (m, 2H), 7.11 (d, J=8.38 Hz, 1H), 7.04 (t, J=75.00 Hz, 1H), 6.94 (d, J=2.21 Hz, 1H), 6.83 (m, 1H), 5.86-6.02 (m, 1H), 5.47 (s, 1 H), 3.78-3.92 (m, 1H), 3.56-3.68 (m, 1H), 3.37-3.49 (m, 1H), 3.20-3.28 (m, 1H), 2.93-3.09 (m, 4H), 2.89 (s, 3H), 2.66 (m 1H).

Example 23 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(cyclopropylmethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (264)

3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (150 mg, 0.262 mmol) was dissolved in MeOH (10 ml), and cyclopropanecarbaldehyde (19.60 μl, 0.262 mmol) was added followed by sodium cyanoborohydride (33.0 mg, 0.525 mmol). The resulting mixture was stirred at RT for 2 hours. The volatiles were removed under reduced pressure, and the residue was purified by preparative HPLC (Method 2). A further purification by flash chromatography on silica gel (DCM/MeOH=99/1) was required to afford 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(cyclopropylmethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (25 mg, 0.042 mmol, 16.17% yield). MS/ESI⁺ 588.94 [MH]⁺; t_(R) (Method 3)=3.54; Diastereomeric Ratio=>95:5 (¹H NMR); [α_(D)]=−30.1 (c=0.31, DCM);

¹H NMR (B) (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2H), 7.19 (d, 1H), 7.13 (d, 1H), 6.97 (dd, 1H), 7.08 (t, 1H), 5.95 (dd, 1H), 4.96 (s, 1H), 3.93 (d, 2H), 3.38-3.56 (m, 1H), 3.40 (dd, 1H), 3.26 (dd, 1H), 2.98-3.17 (m, 1H), 2.76-2.95 (m, 2H), 2.31 (dd, 1H), 2.17 (dd, 1H), 1.14-1.35 (m, 1H), 0.72-0.98 (m, 1H), 0.53-0.66 (m, 2H), 0.43-0.53 (m, 2H), 0.26-0.42 (m, 2H), −0.03-0.19 (m, 2H)

The compounds listed in Table 18 were prepared according to analogous procedure as that described for Scheme 30 and by reacting the appropriate precursors listed with commercial suitable reagents, followed by appropriate purification step as below reported.

TABLE 18 HPLC-MS characterization MS/ t_(R)/min ESI⁺ Method Diastereomeric Purification Starting Entry Structure SALT NAME [MH]⁺ 1, 2 or 3 ratio ¹H NMR [α]_(D) Precursor Method aldehyde 265

Free Base 625.11 4.36 (3) >95:5  (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.46 (s, 2 H), 7.24-7.44 (m, 5 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 6.95(dd, 1 H), 7.08 (t, 1 H), 5.92 (dd, 1 H), 4.73 (s, 1 H), 3.91 (d, 2 H), 3.57 (d, 1 H), 3.51 (d, 1 H), 3.32-3.43 (m, 2 H), 3.21 (dd, 1 H), 3.05-3.17 (m, 1 H), 2.79-3.04 (m, 2 H), 1.05-1.38 (m, 1 H), 0.48-0.72 (m, 2 H), 0.21-0.43 (m, 2 H) +1.3 (c = 0.51; DCM)  6 Preparative HPLC (Method 2)

266

Free Base 696.27 3.79 (3) >95:5  (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.50 (s, 2 H), 7.28-7.49 (m, 4 H), 7.18 (d, 1 H), 7.10 (d, 1 H), 6.94 (dd, 1 H), 7.07 (t, 1 H), 5.90 (dd, 1 H), 4.78 (s, 1 H), 3.91 (d, 2 H), 3.59 (s, 2 H), 3.32-3.44 (m, 2 H), 3.22 (dd, 1 H), 3.06-3.17 (m, 1 H), 2.81-3.05 (m, 8 H), 1.06-1.33 (m, 1 H), 0.45-0.71 (m, 2 H), 0.21-0.45 (m, 2 H) +4.0 (c = 0.9, DCM)  6 Preparative HPLC (Method 2)

267

Free Base 639.37 4.25 (minor) 4.34 (major) (3)   85:15 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.14-7.32 (m, 6 H), 7.11 (d, 1 H), 6.94 (dd, 1 H), 7.08 (t, 1 H), 5.93 (dd, 1 H), 4.93 (s, 1 H), 3.91 (d, 2 H), 3.45-3.52 (m, 1 H), 3.40 (dd, 1 H), 3.25 (dd, 1 H), 2.98-3.15 (m, 1 H), 2.69-2.90 (m, 4 H), 2.54-2.68 (m, 2 H), 1.02-1.34 (m, 1 H), 0.48-0.66 (m, 2 H), 0.16-0.42 (m, 2 H)  6 Preparative HPLC (Method 2)

268

Trifluoroacetate 692.39 2.99 (3)   90:10 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 9.70 (br. s., 1 H), 8.59 (s, 2 H), 7.42-7.62 (m, 4 H), 7.22 (d, 1 H), 7.13 (d, 1 H), 7.01 (dd, 1 H), 7.07 (t, 1 H), 6.03 (dd, 1 H), 4.59 (d, 1 H), 4.08-4.37 (m, 1 H), 3.93(d, 2 H), 3.69-3.84 (m, 1 H), 3.37-3.49 (m, 2 H), 3.10-3.33 (m, 2 H), 2.99 (br. s., 3 H), 2.89 (br. s., 3 H), 2.58-2.77 (m, 1 H), 2.54-2.61 (m, 1 H), 2.09-2.25 (m, 1 H), 1.71-2.09 (m, 2 H), 1.42-1.64 (m, 1 H), 1.08-1.33 (m, 1 H), 0.47-0.70 (m, 2 H), 0.27-0.44 (m, 2 H) −7.7 (c = 0.25, DCM) 179 Preparative HPLC (Method 2)

Example 24 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-ureidophenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (269)

4-((S)-2-((S)-3-(3-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide

140 (140, prepared as described in Example 10, 210 mg, 0.304 mmol), was dissolved in a mixture of AcOH (4 ml) and water (2 ml) at 10° C., and potassium cyanate (99 mg, 1.216 mmol) was immediately added. The reaction was stirred for 1 hour at 10° C. Water was added (30 ml), and the precipitate was collected by filtration and purified by preparative HPLC (Method 2) to afford 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-ureidophenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (136 mg, 0.185 mmol, 61.0% yield). MS/ESI⁺ 733.05 [MH]⁺; t_(R) (Method 3)=5.39; Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−78.85 (c=0.4, DCM);

¹H NMR (B) (300 MHz, DMSO-d₆) δ ppm 8.95 (s, 1H), 8.58 (s, 2H), 8.08 (t, 1H), 7.62 (ddd, 1H), 7.49 (t, 1H), 7.36 (dt, 1H), 7.18 (d, 1H), 7.12 (d, 1H), 6.96 (dd, 1H), 7.08 (t, 1H), 6.02 (dd, 1H), 6.01 (br. S., 2H), 5.30 (s, 1H), 3.91 (d, 2H), 3.61-3.82 (m, 2 H), 3.49-3.54 (m, 1H), 3.31 (dd, 1H), 2.99 (dt, 1H), 2.73 (dt, 1H), 1.09-1.38 (m, 1H), 0.48-0.62 (m, 2H), 0.21-0.45 (m, 2H)

Example 25 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (271)

Step 1: 3-(hydroxymethyl)benzene-1-sulfonyl chloride (270)

To a solution of 3-(chlorosulfonyl)benzoic acid (0.300 g, 1.360 mmol) in dry THF (6 ml) cooled at 0° C., BH3*THF complex 1M in THF (5.44 ml, 5.44 mmol) was added. and the resulting mixture was left to warm to RT and stirred overnight. Additional BH3*THF complex 1M in THF (1.360 ml, 1.360 mmol) was added, and the stirring was continued for 3 days at RT. The mixture was carefully quenched with 2M HCl, diluted with brine and extracted twice with EtOAc. The combined organic layers were washed with brine and dried over sodium sulfate. The solvent was removed and the crude was purified by filtration through a silica gel cartridge (petroleum ether:EtOAc=70:30) affording 3-(hydroxymethyl)benzene-1-sulfonyl chloride (0.086 g, 0.416 mmol, 30.6% yield). MS/ESI⁺ not detectable [MH]⁺.

Step 2: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (271)

To a solution of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (0.183 g, 0.320 mmol) in DCM (5 ml), CH₃CN (2 ml), and pyridine (0.078 ml, 0.960 mmol) cooled at 0° C., a solution of 3-(hydroxymethyl)benzene-1-sulfonyl chloride (0.086 g, 0.416 mmol) in DCM (2 ml) was added, and the resulting mixture was warmed to RT and stirred. The volatiles were removed under vacuum; the residue was purified by preparative HPLC (Method 2 under neutral conditions, whithout TFA) and the collected fractions were frozen dry to afford 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (0.100 g, 0.142 mmol, 44.3% yield); MS/ESI⁺ 705.14 [MH]⁺; t_(R) (Method 3)=3.78; Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−65.67 (c=0.42; MeOH);

¹H NMR (B) (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2H), 7.83 (t, 1H), 7.73 (dt, 1H), 7.68 (dt, 1H), 7.61 (t, 1H), 7.19 (d, 1H), 7.12 (d, 1H), 6.97 (dd, 1H), 7.08 (t, 1H), 6.03 (dd, 1H), 5.44 (t, 1H), 5.38 (s, 1H), 4.62 (d, 2H), 3.91 (d, 2H), 3.76 (dt, 1H), 3.67 (dt, 1H), 3.47 (dd, 1H), 3.31 (dd, 1H), 2.98 (dt, 1H), 2.68 (dt, 1H), 1.03-1.38 (m, 1H), 0.49-0.67 (m, 2H), 0.15-0.45 (m, 2H).

Example 26 Synthesis of 4-((2S)-2-(2-(3-benzoylthiazolidin-2-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (274)

Step 1: ethyl 2-(3-benzoylthiazolidin-2-yl]acetate (272)

A mixture of ethyl 2-(thiazolidin-2-yl)acetate (0.100 g, 0.571 mmol) (prepared following the synthetic protocol described in J. Chem. Soc. Perkin Trans. I, 1987, 1845-1851, which is incorporated herein by reference in its entirety), benzoic acid (0.084 g, 0.685 mmol), EDC (0.219 g, 1.141 mmol), and DMAP (0.070 g, 0.571 mmol) in DCM (10 ml) was stirred at RT for 1 hour. The mixture was diluted with DCM and washed with aqueous 1N HCl, 1N NaHCO₃ and brine; the organic phase was dried over sodium sulfate and the solvent was removed. The residue was purified by flash chromatography on silica gel cartridge (petroleum ether:EtOAc=80:20 to 70:30) yielding ethyl 2-(3-benzoylthiazolidin-2-yl)acetate (0.085 g, 0.304 mmol, 53% yield). MS/ESI⁺ 280.0 [MH]⁺.

Step 2: 2-(3-benzoylthiazolidin-2-yl)acetic acid (273)

To a solution of ethyl 2-(3-benzoylthiazolidin-2-yl)acetate (0.083 g, 0.297 mmol) in dioxane (4 ml), aqueous 37% HCl (4 ml) was added, and the mixture was stirred at RT for 20 hours. The volatiles were removed under vacuum yielding crude 2-(3-benzoylthiazolidin-2-yl)acetic acid (0.074 g, 0.294 mmol, 99% yield) which was used without purification. MS/ESI⁺ 251.9 [MH]⁺.

Step 3: 4-((2S)-2-(2-(3-benzoylthiazolidin-2-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide (274)

A mixture of 2-(3-benzoylthiazolidin-2-yl)acetic acid (0.074 g, 0.294 mmol), (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (0.103 g, 0.245 mmol), EDC (0.141 g, 0.736 mmol), and DMAP (0.030 g, 0.245 mmol) in DCM (10 ml) was stirred at RT for 2 hours. The mixture was diluted with DCM and washed with 1N HCl, 1N NaHCO₃ and brine; the organic phase was dried over sodium sulfate and the solvent was removed. The crude was purified by preparative HPLC (Method 2) followed by flash chromatography on silica gel cartridge (DCM:MeOH=99:1) yielding title compound as a distereomeric mixture (0.065 g, 0.099 mmol, 40.5% yield); MS/ESI⁺ 653.19 [MH]⁺; t_(R) (Method 3)=3.92; Diastereomeric Ratio=1:1 (¹H NMR).

The compound listed in Table 19 was prepared according to analogous procedures as those described for Scheme 33 and using suitable reagents, followed by appropriate purification step as below reported.

TABLE 19 HPLC-MS characterization t_(R)/min Diastere- SALT MS/ESI⁺ Method omeric Purification Entry Structure NAME [MH]⁺ 1, 2 or 3 ratio Method 275

Free Base 724.39 3.53 (3) 1:1 (¹H NMR) Preparative HPLC (Method 2)

Example 27 Synthesis of 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide (278)

Step 1: ethyl 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetate (276)

To a solution of ethyl 2-(thiazolidin-2-yl)acetate (0.100 g, 0.571 mmol) (prepared following the synthetic protocol described in J. Chem. Soc. Perkin Trans. I, 1987, 1845-1851, which is incorporated herein by reference in its entirety) in pyridine (4 ml) cooled at 0° C., benzenesulfonyl chloride (0.088 ml, 0.685 mmol) was added, and the reaction was stirred for 2 hours at RT. The mixture was partitioned between EtOAc and 1N HCl; the organic phase was washed with 1N HCl and brine and dried over sodium sulfate. The solvent was removed and the crude was purified by flash chromatography on silica gel (petroleum ether:EtOAc=90:10 to 80:20) affording ethyl 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetate (0.096 g, 0.304 mmol, 53.3% yield). MS/ESI⁺ 316.0 [MH]⁺.

Step 2: 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetic acid (277)

To a solution of ethyl 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetate (0.096 g, 0.304 mmol) in dioxane (5 ml), aqueous 37% HCl (5 ml) was added, and the mixture was stirred at RT for 25 hours. The volatiles were removed under vacuum to afford 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetic acid (0.083 g, 0.289 mmol, 95% yield) which was used without purification. MS/ESI⁺ 310.0 [Mna]⁺.

Step 3: 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide (278)

A mixture of 2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetic acid (0.083 g, 0.289 mmol), (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (0.101 g, 0.241 mmol), EDC (0.046 g, 0.241 mmol), and DMAP (0.029 g, 0.241 mmol) in DCM (10 ml) was stirred at RT for 1 hour. The mixture was diluted with DCM and washed with 1N HCl, 1N NaHCO₃ and brine; the organic phase was dried over sodium sulfate and the solvent was removed. The crude was purified by preparative HPLC (Method 2) affording 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide (0.122 g, 0.177 mmol, 73.5% yield); MS/ESI⁺ 689.14 [MH]⁺; t_(R) (Method 3)=4.09; Diastereomeric Ratio=1:1 (¹H NMR).

The compound listed in Table 20 was prepared according to analogous procedures as those described for Scheme 42 and using suitable reagents, followed by appropriate purification step as below reported.

TABLE 20 HPLC-MS characterization t_(R)/min Diastere- SALT MS/ESI⁺ Method omeric Purification Entry Structure NAME [MH]⁺ 1, 2 or 3 ratio Method 279

Free Base 760.23 3.67 (3) 1:1 (¹H NMR) Flash chromatography on silica gel

Example 28 (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carbonyloxy)ethyl)pyridine 1-oxide (281)

Step 1: 1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carboxylic acid (280)

To a suspension of azetidine-3-carboxylic acid (100 mg, 0.989 mmol) in a mixture of THF (6 ml) and aqueous 1M Na₂CO₃ (6 ml, 6.00 mmol) cooled at 0° C., 3-(dimethylcarbamoyl)benzene-1-sulfonyl chloride (269 mg, 1.088 mmol) was added, and the reaction was stirred at 0° C. for 1 hour. The mixture was extracted with Et₂O, and the organic layer was discarded. The aqueous layer was carefully acidified by addition of solid KHSO₄ (pH=3) and extracted twice with EtOAc. The combined organic layers were dried over Na₂SO₄ and evaporated to dryness yielding crude 1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carboxylic acid (255 mg, 0.816 mmol, 83% yield) which was used without purification.

MS/ESI⁺ 313.12 [MH]

Step 2: (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carbonyloxy)ethyl)pyridine 1-oxide (281)

A solution of 1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carboxylic acid (255 mg, 0.816 mmol), (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (175 mg, 0.416 mmol), EDC (96 mg, 0.500 mmol), and DMAP (61.0 mg, 0.500 mmol) in DCM (30 ml) was stirred at RT overnight. More EDC (80 mg, 0.416 mmol) and DMAP (61.0 mg, 0.500 mmol) were added, and the stirring was continued for further 2 hours. The reaction mixture was washed twice with aqueous 1N HCl then with aqueous 1M Na₂CO₃, the organic phase was dried over Na₂SO₄ and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC (Method 2) to afford (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carbonyloxy)ethyl)pyridine 1-oxide (192 mg, 0.269 mmol, 64.5% yield); MS/ESI⁺ 714.16 [MH]⁺; [α_(n)]=−14.3 (c=0.37, DCM); ¹H NMR (B) (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2H), 7.68-7.90 (m, 4H), 7.16 (d, 1 H), 7.02 (d, 1H), 6.85 (dd, 1H), 7.07 (t, 1H), 5.82 (dd, 1H), 3.85-4.06 (m, 2H), 3.89 (d, 2H), 3.71 (dd, 1H), 3.56 (dd, 1H), 3.42-3.49 (m, 2H), 3.14 (dd, 1H), 3.01 (br. S., 3H), 2.86 (br. S., 3H), 1.02-1.37 (m, 1H), 0.50-0.78 (m, 2H), 0.07-0.50 (m, 2H)

The compounds listed in Table 21 were prepared according to analogous procedures as those described for Scheme 34 and by reacting the appropriate aminoacid precursor listed with commercial suitable reagents, followed by appropriate purification step as below reported, if needed. For the preparation of compound 283 and compound 284, Step 1 was accomplished using water as the solvent.

TABLE 21 HPLC-MS characterization MS/ t_(R)/min ESI⁺ Method Diastereomeric Purification Sulfonyl Entry Structure SALT NAME [MH]⁺ 1, 2 or 3 ratio ¹H NMR [α]_(D) Precursor Method aldehyde 282

Free Base 643.14 3.93 (3) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.60-7.85 (m, 5 H), 7.16 (d, 1 H), 7.02 (d, 1 H), 6.84 (dd, 1 H), 7.07 (t, 1 H), 5.82 (dd, 1 H), 3.89 (d, 2 H), 3.84-3.98 (m, 2 H), 3.69 (dd, 1 H), 3.51 (dd, 1 H), 3.36-3.47 (m, 2 H), 3.13 (dd, 1 H), 1.08-1.39 (m, 1 H), 0.47-0.67 (m, 2 H), 0.20-0.44 (m, 2 H) −10.9  (c = 0.48, DCM)

Preparative HPLC (Method 2)

283

Free Base 714.14 6.74 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57 (s, 2 H), 7.65-7.90 (m, 4 H), 7.18 (d, 1 H), 7.14 (d, 1 H), 6.96 (dd, 1 H), 7.07 (t, 1 H), 6.03 (dd, 1 H), 4.50 (dd, 1 H), 3.91 (d, 2 H), 3.68-3.80 (m, 1 H), 3.59-3.68 (m, 1 H), 3.47 (dd, 1 H), 3.20-3.27 (m, 1 H), 3.02 (br. S., 3 H), 2.92 (br. S., 3 H), 2.19-2.39 (m, 1 H), 2.02-2.19 (m, 1 H), 1.03-1.34 (m, 1 H), 0.47-0.64 (m, 2 H), 0.15-0.43 (m, 2 H) −73.97 (c = 1.2, DCM)

Preparative HPLC (Method 2)

284

Free Base 643.23 3.93 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.59 (s, 2 H), 7.74-7.89 (m, 3 H), 7.61-7.74 (m, 2 H), 7.18 (d, 1 H), 7.14 (d, 1 H), 6.96 (dd, 1 H), 7.08 (t, 1 H), 6.03 (dd, 1 H), 4.42 (dd, 1 H), 3.91 (d, 2 H), 3.65-3.78 (m, 1 H), 3.55-3.67 (m, 1 H), 3.47 (dd, 1 H), 3.21-3.26 (m, 1 H), 2.13-2.26 (m, 1 H), 1.91-2.15 (m, 1 H), 1.05-1.34 (m, 1 H), 0.48-0.63 (m, 2 H), 0.24-0.41 (m, 2 H) −85.36 (c = 0.53, DCM)

Trituration with MeOH

285

Free Base 726.1 3.66 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.60 (s, 2 H), 7.71 (dd, 1 H), 7.64 (d, 1 H), 7.19 (d, 1 H), 7.18 (d, 1 H), 7.14 (d, 1 H), 6.99 (dd, 1 H), 7.08 (t, 1 H), 6.04 (dd, 1 H), 4.10 (dd, 1 H), 3.93 (d, 2 H), 3.69 (s, 2 H), 3.32-3.58 (m, 3 H), 3.18 (s, 3 H), 2.99-3.26 (m, 1 H), 1.80-2.10 (m, 1 H), 1.60-1.80 (m, 2 H), 1.54 (d, 1 H), 0.93-1.32 (m, 1 H), 0.44-0.71 (m, 2 H), 0.05-0.44 (m, 2 H) −48.1  (c = 0.46, DCM)

Flash chromatography on silica gel

Example 29 Synthesis of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-morpholinoethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (287)

Step 1: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(vinylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (286)

To a solution of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (500 mg, 0.874 mmol) in DCM (10 ml) cooled at 0° C., pyridine (212 μl, 2.62 mmol) and 2-chloroethanesulfonyl chloride (137 μl, 1.312 mmol) were added, and the mixture was left to warm to RT and stirred for 2 hours. Additional pyridine (707 μl, 8.74 mmol) and 2-chloroethanesulfonyl chloride (137 μl, 1.312 mmol) were added at 0° C., and the mixture reacted for 6 hours at RT. The mixture was diluted with DCM and washed with 1N HCl and brine; the organic layer was dried over Na₂SO₄ and the solvent was removed under vacuum. The resulting crude was purified by flash chromatography on silica gel (DCM/MeOH=98/2) yielding 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(vinylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (360 mg, 0.576 mmol, 66% yield); MS/ESI⁺ 624.9 [MH]⁺.

Step 2: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-morpholinoethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (287)

To a solution of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(vinylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (110 mg, 0.176 mmol) in EtOH (5 ml), morpholine (35.2 μl, 0.352 mmol) was added and the mixture was reacted at RT for 1 hour. The solvent was removed under reduced pressure, and the crude was purified by preparative HPLC (Method 3) yielding 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(vinylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide as trifluoroacetate salt; MS/ESI⁺ 712.14 [MH]⁺; t_(R) (Method 3)=3.16; Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−126.6 (c=0.23 DCM);

¹H NMR (B) (300 MHz, DMSO-d₆) δ ppm 8.55 (s, 2H), 7.19 (d, 1H), 7.11 (d, 1H), 6.97 (dd, 1H), 7.08 (t, 1H), 6.03 (dd, 1H), 5.58 (s, 1H), 3.94-4.02 (m, 1H), 3.91 (d, 2H), 3.61-3.74 (m, 1H), 3.45 (dd, 1H), 3.31 (dd, 1H), 3.06-3.81 (m, 12H), 3.00-3.25 (m, 2H), 1.03-1.35 (m, 1H), 0.47-0.70 (m, 2H), 0.10-0.45 (m, 2H)

The compound listed in Table 22 was prepared according to analogous procedures as those described for Scheme 35 and by reacting the appropriate precursor listed with commercial suitable reagents, followed by appropriate purification step.

TABLE 22 HPLC-MS characterization t_(R)/min Dia- Meth- stereo- Pre- Purifi- SALT MS/ESI⁺ od 1, meric cur- cation Entry Structure NAME [MH]⁺ 2 or 3 ratio ¹H NMR [α]_(D) sor Method Amine 288

Tri- fluoro- acetate (mono salt) 725.15 3.09 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.58 (s, 2 H), 7.60-7.85 (m, 5 H), 7.16 (d, 1 H), 7.02 (d, 1 H), 6.84 (dd, 1 H), 7.07 (t, 1 H), 5.82 (dd, 1 H), 3.89 (d, 2 H), 3.84-3.98 (m, 2 H), 3.69 (dd, 1 H), 3.51 (dd, 1 H), 3.36-3.47 (m, 2 H), 3.13 (dd, 1 H), 1.08-1.39 (m, 1 H), 0.47-0.67 (m, 2 H), 0.20-0.44 (m, 2 H) −80.24 (c = 0.325, DCM) 6 Prepar- ative HPLC (Method 3)

Example 30 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (291)

Step 1: (S)-benzyl 1-(2-(phenylsulfonypethyl)pyrrolidine-2-carboxylate (289)

A solution of (S)-benzyl pyrrolidine-2-carboxylate hydrochloride (250 mg, 1.034 mmol), vinylsulfonylbenzene (261 mg, 1.551 mmol), and TEA (0.216 ml, 1.551 mmol) in EtOH (15 ml) was stirred at RT for 24 hours. The reaction mixture was then diluted with DCM (50 ml) and washed twice with aqueous sat. NH₄Cl. The organic layer was dried over Na₂SO₄ and the solvent was removed under vacuum. The residue was dissolved in DCM (15 ml) and EtOH (15 ml), and PS-trisamine (free —NH₂ group: 4.7 mmol/g, 0.5 g, 0.35 mmol) was added. The suspension was stirred at RT for 3 days. The resin was filtered off and the solution evaporated to dryness to afford the desired product (379 mg, 1.01 mmol, 98% yield). MS/ESI⁺ 374.10 [MH]⁺.

Step 2: (S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carboxylic acid (290)

A suspension of 10% Pd/C (10.80 mg, 0.101 mmol) in water (2 ml) was added to a solution of (S)-benzyl 1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carboxylate (379 mg, 1.015 mmol) in MeOH (15 ml). The mixture was hydrogenated in a Parr apparatus at 30 psi for 1 hour at RT. The catalyst was filtered off and the resulting clear solution was evaporated to dryness to afford the desired product (272 mg, 0.860 mmol, 95% yield).

MS/ESI⁺ 284.02 [MH]⁺.

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (291)

A solution of (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-hydroxyethyl)pyridine 1-oxide (150 mg, 0.357 mmol), (S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carboxylic acid (152 mg, 0.535 mmol), EDC (103 mg, 0.535 mmol), and DMAP (21.80 mg, 0.178 mmol) in DCM (30 ml) was stirred at RT for 1 hour. The reaction mixture was washed twice with 1N HCl, dried over Na₂SO₄ and evaporated to dryness. The residue was purified by preparative HPLC (Method 2), and the collected fractions were evaporated to dryness, redissolved DCM and eluted through a PL-HCO₃ cartridge (200 mg, 0.36 mmoles). The eluted solution was evaporated to dryness affording title compound (110 mg, 0.160 mmol, 45% yield); [α_(D)]=−33.8 (c=0.44, DCM); MS/ESI⁺ 685.42 [MH]⁺; t_(R)=3.15 min (Method 3); Diastereomeric Ratio >95:5 ('H NMR);

¹H NMR (B) (300 MHz, DMSO-d6) δ ppm 8.55 (s, 2H), 7.83-7.98 (m, 2H), 7.69-7.82 (m, 1H), 7.53-7.69 (m, 2H), 7.17 (d, 1H), 7.06 (d, 1H), 6.93 (dd, 1H), 7.06 (t, 1 H), 5.92 (dd, 1H), 3.80-4.04 (m, 2H), 3.43-3.58 (m, 1H), 3.41 (dd, 1H), 3.23 (dd, 1 H), 2.61-3.09 (m, 5H), 2.25-2.44 (m, 1H), 1.84-2.08 (m, 1H), 1.37-1.78 (m, 3H), 1.09-1.33 (m, 1H), 0.48-0.73 (m, 2H), 0.25-0.43 (m, 2H)

Example 31 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (292)

To a solution of 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (6) (200 mg, 0.361 mmol) and pyridine (292 μl, 3.61 mmol) in dry DCM (5 ml), a solution of phenyl-acetyl chloride (84 mg, 0.542 mmol) in dry DCM (1 ml) was added dropwise at 0° C. and the mixture was left to warm to RT and stirred for 2 hours. EtOAc (20 ml) was added, and the mixture was washed with aqueous 5% citric acid and brine; the organic phase was dried over Na₂SO₄, filtered and evaporated. The residue was purified by flash chromatography on silica gel (DCM/MeOH=95/5). A further purification by preparative HPLC (Method 2) was required to afford 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (35 mg, 0.055 mmol, 15.25% yield); MS/ESI⁺ 635.23 [MH]⁺; t_(R)=3.91 min (Method 3); Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−28.26 (c=0.23, MeOH);

¹H NMR (B) (300 MHz, DMSO-d₆ 353K) δ ppm 8.40 (s, 2H), 7.16-7.39 (m, 5H), 7.13 (d, 1H), 7.08 (d, 1H), 6.89-6.95 (m, 1H), 6.97 (t, 1H), 5.85-6.08 (m, 1H), 4.26-4.45 (m, 1H), 3.91 (d, 2H), 3.66 (br. S., 2H), 3.47-3.63 (m, 3H), 3.27 (dd, 1H), 2.01-2.25 (m, 1H), 1.83-1.99 (m, 1H), 1.49-1.83 (m, 2H), 1.07-1.26 (m, 1H), 0.44-0.69 (m, 2H), 0.19-0.40 (m, 2H)

Example 32 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzylsulfonyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (295)

Step 1: (3-(dimethylcarbamoyl)phenyl)methanesulfonic acid (293)

To a suspension of 3-(chloromethyl)-N,N-dimethylbenzamide (1.15 g, 5.82 mmol) in water (30 ml), sodium sulfite (1.100 g, 8.73 mmol) was added, and the mixture was heated at 100° C. for 1 hour. The solvent was removed under vacuum, and the residue was suspended in MeOH (40 ml). HCl 4M in dioxane (5 ml) was added, and the insoluble inorganic salts were filtered off. The filtrate was evaporated to dryness and the residue was purified by several trituration with CH₃CN affording (3-(dimethylcarbamoyl)phenyl)methanesulfonic acid (1.04 g, 4.27 mmol, 73.5% yield).

MS/ESI⁺ 243.95 [MH]

Step 2: (3-(dimethylcarbamoyl)phenyl)methanesulfonyl chloride (294)

To a suspension of (3-(dimethylcarbamoyl)phenyl)methanesulfonic acid (500 mg, 2.055 mmol) in DCM (40 ml), thionyl chloride (0.900 ml, 12.33 mmol) was added, and the resulting mixture was stirred at RT for 20 hours. The reaction mixture was poured into crushed ice and the organic phase was separated and dried over Na₂SO₄. The solvent was removed under vacuum to afford desired product (357 mg, 1.364 mmol, 66% yield).

MS/ESI⁺ 261.96 [MH]⁺

Step 3: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzylsulfonyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (295) 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoro-methoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzylsulfonyl)-thiazolidine-2-carbonyloxy)ethyl)pyridine

1-oxide was obtained according to analogous procedure as that described for Scheme 16 (Example 8). It was purified by treatment with polymer supported isocyanate scavenger followed by preparative HPLC (Method 2) (20% yield); MS/ESI⁺ 760.17 [MH]⁺, t_(R)=3.78 min (Method 3); Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−15.8 (c=3.0, DCM);

¹H NMR (B) (300 MHz, DMSO-d6) 8 ppm 8.53 (s, 2H), 7.38-7.55 (m, 4H), 7.17 (d, 1 H), 7.08 (d, 1H), 6.94 (dd, 1H), 7.07 (t, 1H), 6.00 (dd, 1H), 5.27 (s, 1H), 4.67 (d, 1H), 4.61 (d, 1H), 3.85-3.98 (m, 2H), 3.74-3.85 (m, 1H), 3.51-3.66 (m, 1H), 3.36-3.50 (m, 2H), 3.20-3.26 (m, 1H), 3.04-3.14 (m, 1H), 2.99 (br. S., 3H), 2.92 (br. S., 3 H), 1.04-1.42 (m, 1H), 0.46-0.66 (m, 2H), 0.20-0.41 (m, 2H)

The compound listed in Table 23 was obtained according to analogous procedures as those described for Scheme 38, and by reacting the appropriate precursor, obtained as free base after basic treatment of hydrochloride salt with aqueous sat. NaHCO₃ followed by extraction with DCM. The purification step is described below.

TABLE 23 HPLC-MS characterization t_(R)/min Dia- Meth- stereo- Pre- Purifi- SALT MS/ESI⁺ od 1, meric cur- cation Entry Structure NAME [MH]⁺ 2 or 3 ratio ¹H NMR [α]_(D) sor Method 296

Free Base 742.30 3.61 (3) >95:5 (¹H NMR B) 11H NMR (300 MHz, DMSO-d6) δ ppm 8.54 (s, 2 H), 7.36-7.54 (m, 4 H), 7.16 (d, 1 H), 7.10 (d, 1 H), 6.94 (dd, 1 H), 7.06 (t, 1 H), 5.98 (dd, 1 H), 4.54 (d, 1 H), 4.46 (d, 1 H), 4.07 (dd, 1 H), 3.83- 3.97 (m, 2 H), 3.42 (dd, 1 H), 3.27-3.36 (m, 2 H), 3.23 (dd, 1 H), 2.98 (br. S., 3 H), 2.91 (br. S., 3 H), 2.00- 2.24 (m, 1 H), 1.57- 1.95 (m, 3 H), 0.93- 1.31 (m, 1 H), 0.45- 0.64 (m, 2H), 0.12- 0.44 (m, 2 H) −8.7 (c 0.33 in DCM) Free Base of 3 Prepar- ative HPLC (Method 2)

Example 33 Synthesis of 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (299)

Step 1: 4-((S)-2-((S)-3-(tert-butoxycarbonyl)thiazolidine-2-carbonyloxy)-2-(4-(difluoromethoxy)-3-methoxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (297)

A solution of (S)-3-(tert-butoxycarbonyl)thiazolidine-2-carboxylic acid (479 mg, 2.052 mmol), (S)-3,5-dichloro-4-(2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (164) (prepared according to analogous procedure as that described for Scheme 23), (650 mg, 1.710 mmol), EDC (492 mg, 2.56 mmol), and DMAP (313 mg, 2.56 mmol) in DCM (60 ml) was stirred at RT for 3 hours. The reaction mixture was diluted with DCM and washed twice with aqueous 1N HCl; the organic layer was dried over Na₂SO₄ and evaporated to dryness to afford the desired compound (quantitative yield). MS/ESI⁺ 595.24 [MH]⁺.

Step 2: 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (298)

To a solution of 4-((S)-2-((S)-3-(tert-butoxycarbonyl)thiazolidine-2-carbonyloxy)-2-(4-(difluoromethoxy)-3-methoxyphenyl)ethyl)-3,5-dichloropyridine 1-oxide (1.710 mmol) in EtOAc (10 ml) cooled at 0° C., HCl, 4M solution in EtOAc (10 ml, 40.0 mmol) was added, and the resulting mixture was stirred at RT for 2 hours. More HCl, 4M solution in EtOAc (10 ml, 40.0 mmol) was added, and the solution was stirred at 0° C. for additional 2 hours to reach complete conversion. The solution was concentrated to 10 ml under reduced pressure (bath temperature: 10° C.; partial pressure: 8 psi), then iPr₂O (20 ml) was added and the product precipitated as a sticky gummy solid. After the solid was allowed to settle down, the solvent was removed by aspiration. The residue was dried in vacuo at RT to afford 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (0.890 g, 1.674 mmol, 97% yield), which was employed in the next step without any additional purification. MS/ESI⁺ 494.97 [MH].

Step 3: 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (299)

To a solution of 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide hydrochloride (350 mg, 0.658 mmol) in pyridine (6 ml) cooled at 0° C., a solution of 3-(dimethylcarbamoyl)benzene-1-sulfonyl chloride (245 mg, 0.987 mmol) in DCM (3 ml) was added drop-wise, and the reaction was stirred at 0° C. for 1 hour. The mixture was diluted with DCM (30 ml) and washed twice with aqueous 1N HCl; the organic layer was dried over Na₂SO₄ and the solvent was removed under vacuum. The residue was purified by preparative HPLC (Method 2) followed by flash chromatography on silica gel (DCM/MeOH=97/3) to afford 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (147 mg, 0.208 mmol, 31.6% yield); MS/ESI⁺ 705.97 [MH]⁺, t_(R)=3.28 min (Method 3); Diastereomeric Ratio=95:5 (¹H NMR); [α_(D)]=−43.1 (c=0.57, DCM);

¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.57 (s, 2H), 7.94 (dt, 1H), 7.90 (t, 1H), 7.77 (dt, 1H), 7.71 (t, 1H), 7.18 (d, 1H), 7.15 (d, 1H), 6.97 (dd, 1H), 7.07 (t, 1H), 6.04 (dd, 1 H), 5.54 (s, 1H), 3.84 (s, 3H), 3.75-3.94 (m, 1H), 3.66 (dt, 1H), 3.48 (dd, 1H), 3.33 (dd, 1H), 3.02 (br. S., 3H), 2.98 (dd, 1H), 2.90 (br. S., 3H), 2.66 (dt, 1H)

The compounds listed in Table 24 were prepared according to analogous procedures as those described for Scheme 39 and by reacting the appropriate alcohol listed with commercial suitable reagents, followed by appropriate purification step as below reported. Compound 303 was obtained as second eluted diastereoisomer from a mixture of diastereoisomers

TABLE 24 HPLC-MS characterization t_(R)/min Dia- Meth- stereo- Purifi- SALT MS/ESI⁺ od 1, meric Alco- cation Entry Structure NAME [MH]⁺ 2 or 3 ratio ¹H NMR [α]_(D) hol Method 300

Free Base 653.03 3.69 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.59 (s, 2 H), 7.83-7.93 (m, 2 H), 7.71-7.81 (m, 0 H), 7.58-7.71 (m, 2 H), 7.19 (d, 1 H), 7.15 (d, 1 H), 6.97 (dd, 1 H), 7.08 (t, 1 H), 6.04 (dd, 1 H), 5.44 (s, 1 H), 3.85 (s, 3 H), 3.81 (dt, 1 H), 3.65 (dt, 1 H), 3.48 (dd, 1 H), 3.32 (dd, 1 H), 2.99 (dt, 1 H), 2.66 (dt, 1 H) −51.1 (c = 0.52, DCM) 164 Prepar- ative HPLC (Method 2) 301

Free Base 689.13 4.37 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.58 (s, 2 H), 7.84-7.97 (m, 2 H), 7.72-7.83 (m, 1 H), 7.59-7.70 (m, 2 H), 7.17 (d, 1 H), 7.08 (d, 1 H), 6.94 (dd, 1 H), 7.00 (t, 1 H), 6.02 (dd, 1 H), 5.46 (s, 1 H), 4.69-5.06 (m, 1 H), 3.82 (dt, 1 H), 3.64 (dt, 1 H), 3.46 (dd, 1 H), 3.31 (dd, 1 H), 2.98 (dt, 1 H), 2.65 (dt, 1 H), 1.42-2.03 (m, 8 H) −43.0 (c = 0.53; DCM) 165 Prepar- ative HPLC (Method 2) 302

Free Base 760.17 3.98 (3) 95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.57 (s, 2 H), 7.95 (dt, 1 H), 7.91 (t, 1 H), 7.77 (dt, 1 H), 7.72 (td, 1 H), 7.16 (d, 1 H), 7.08 (d, 1 H), 6.94 (dd, 1 H), 6.99 (t, 1 H), 6.02 (dd, 1 H), 5.57 (s, 1 H), 4.82-5.00 (m, 1 H), 3.87 (dt, 1 H), 3.65 (dt, 1 H), 3.46 (dd, 1 H), 3.32 (dd, 1 H), 3.03 (br. S., 3 H), 2.93-3.01 (m, 1 H), 2.90 (br. S., 3 H), 2.65 (dt, 1 H), 1.38- 2.04 (m, 8 H) −42.7 (c = 0.50; DCM) 165 Prepar- ative HPLC (Method 2) 303

Free Base 689.97 3.59 (3) 95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.94 (dt, 1 H), 7.89 (t, 1 H), 7.77 (dt, 1 H), 7.71 (t, 1 H), 7.51 (d, 1 H), 7.43 (d, 1 H), 7.23 (dd, 1 H), 6.04 (dd, 1 H), 5.53 (s, 1 H), 3.83 (dt, 1 H), 3.65 (dt, 1 H), 3.48 (dd, 1 H), 3.31 (dd, 1 H), 3.02 (br. S., 3 H), 2.93- 3.01 (m, 1 H), 2.90 (br. S., 3H), 2.67 (dt, 1 H) −48.68 (c = 0.49, DCM) 172 Prepar- ative HPLC (Method 2)

Example 34 Synthesis of 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (Compound 305)

Step 1: (S)-1-(phenylsulfonyl)pyrrolidine-2-carboxylic acid (304)

Benzenesulfonyl chloride (4.03 ml, 31.3 mmol) was added to a cooled suspension (0° C.) of (S)-pyrrolidine-2-carboxylic acid (3 g, 26.1 mmol) in THF (50 ml) and aqueous 1M Na₂CO₃ (60 ml, 60.0 mmol), and the reaction was stirred at 0° C. for 1 hour. The mixture was extracted twice with Et₂O, and the organic layers were discarded. The aqueous phase was cautiously acidified by addition of solid KHSO₄ to pH=3 and extracted twice with EtOAc. The combined organic layers were dried over Na₂SO₄ and evaporated to dryness to afford (S)-1-(phenylsulfonyl)pyrrolidine-2-carboxylic acid (6.1 g, 23.89 mmol, 92% yield). MS/ESI⁺ 256.10 [MH]

Step 2: 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (305)

A mixture of (S)-3,5-dichloro-4-(2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (164) (55 mg, 0.145 mmol), (S)-1-(phenylsulfonyl)pyrrolidine-2-carboxylic acid (111 mg, 0.434 mmol), EDC (83 mg, 0.434 mmol), and DMAP (53.0 mg, 0.434 mmol) in DCM (20 ml) was stirred at RT for 3 hours. The reaction mixture was washed twice with aqueous 1N HCl and then with aqueous 1M K₂CO₃; the organic layer was dried over Na₂SO₄ and the solvent was removed under reduced pressure. The residue was purified by preparative HPLC (Method 2) to afford 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (45 mg, 0.073 mmol, 50.4% yield); MS/ESI⁺ 617.15 [MH]⁺, t_(R)=3.71 min (Method 3); Diastereomeric Ratio >95:5 (¹H NMR); [α_(D)]=−60.3 (c=0.39, DCM);

¹H NMR (B) (300 MHz, DMSO-d₆) 8 ppm 8.61 (s, 2H), 7.75-7.85 (m, 2H), 7.69-7.76 (m, 1H), 7.56-7.69 (m, 2H), 7.19 (d, 1H), 7.18 (d, 1H), 7.00 (dd, 1H), 7.07 (t, 1 H), 6.05 (dd, 1H), 4.16 (dd, 1H), 3.86 (s, 3H), 3.49 (dd, 1H), 3.39-3.44 (m, 1H), 3.29 (dd, 1H), 3.09-3.23 (m, 1H), 1.83-2.10 (m, 1H), 1.59-1.82 (m, 2H), 1.44-1.59 (m, 1H)

The compounds listed in Table 25 were prepared according to analogous procedures as those described for Scheme 40 using commercial suitable reagents and by reacting the appropriate alcohol listed, followed by appropriate purification step as below reported. Compound 315 was obtained as second eluted diastereoisomer from a mixture of diastereoisomers

TABLE 25 HPLC-MS characterization Alco- t_(R)/min Dia- hol Method stereo- Pre- Purifi- SALT MS/ESI⁺ 1, 2 meric cur- cation Entry Structure NAME [MH]⁺ or 3 ratio ¹H NMR [α]_(D) sor Method 306

Free Base 688.22 3.24 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.58 (s, 2 H), 7.84 (dt, 1 H), 7.64-7.80 (m, 3 H), 7.13-7.26 (m, 2 H), 7.00 (dd, 1 H), 7.07 (t, 1 H), 6.05 (dd, 1 H), 4.21 (dd, 1 H), 3.86 (s, 3 H), 3.50 (dd, 1 H), 3.34-3.44 (m, 1 H), 3.29 (dd, 1 H), 3.20 (dt, 1 H), 3.02 (br. S., 3 H), 2.90 (br. S., 3 H), 1.89- 2.13 (m, 1 H), 1.50- 1.77 (m, 3 H) −56.63 c = 0.47, DCM 164 Prepar- ative HPLC (Method 2) 307

Free Base 671.24 4.32 (3) 80:20 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.60 (s, 2 H), 7.58-7.81 (m, 5 H), 7.17 (d, 1 H), 7.11 (d, 1 H), 6.97 (dd, 1 H), 7.00 (t, 1 H), 6.02 (dd, 1 H), 4.75-5.06 (m, 1 H), 3.99-4.31 (m, 1 H), 3.36-3.55 (m, 2 H), 3.06-3.27 (m, 2 H), 1.81-1.97 (m, 3 H), 1.47-1.79 (m, 9 H) −56.4 c = 0.53, DCM 165 Prepar- ative HPLC (Method 2) 308

Free Base 742.12 3.86 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.57 (s, 2 H), 7.84 (dt, 1 H), 7.72-7.80 (m, 2 H), 7.71 (t, 1 H), 7.17 (d, 1 H), 7.11 (d, 1 H), 6.97 (dd, 1 H), 6.99 (t, 1 H), 6.02 (dd, 1 H), 4.93 (tt, 1 H), 4.22 (dd, 1 H), 3.48 (dd, 1 H), 3.15-3.38 (m, 3 H), 3.02 (br. S., 3 H), 2.90 (br. S., 3 H), 1.42-2.10 (m, 12 H) −55.6, (c = 0.49, DCM 165 Prepar- ative HPLC (Method 2) 309

Free Base 581.15 3.14 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.60 (s, 2 H), 7.74-7.83 (m, 2 H), 7.69-7.74 (m, 1 H), 7.56-7.69 (m, 2 H), 6.98 (d, 1 H), 6.95 (d, 1 H), 6.91 (dd, 1 H), 6.02 (dd, 1 H), 4.14 (dd, 1 H), 3.77 (s, 3 H), 3.76 (s, 3 H), 3.50 (dd, 1 H), 3.33-3.42 (m, 1 H), 3.26 (dd, 1 H), 3.17 (dt, 1 H), 1.77-2.03 (m, 1 H), 1.59-1.77 (m, 2 H), 1.36-1.59 (m, 1 H) −71.5, (c = 0.46, DCM 170 Prepar- ative HPLC (Method 2) 310

Free Base 652.25 2.74 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.57 (s, 2 H), 7.83 (dt, 1 H), 7.60-7.80 (m, 3 H), 6.98 (d, 1 H), 6.95 (d, 1 H), 6.91 (dd, 1 H), 6.02 (dd, 1 H), 4.18 (dd, 1 H), 3.77 (s, 3 H), 3.76 (s, 3 H), 3.50 (dd, 1 H), 3.31-3.42 (m, 1 H), 3.26 (dd, 1 H), 3.12-3.22 (m, 1 H), 3.02 (br. S., 3 H), 2.90 (br. S., 3 H), 1.80-2.06 (m, 1 H), 1.41-1.80 (m, 3 H) −70.4 (c = 0.85, DCM 170 Prepar- ative HPLC (Method 2) 311

Free Base 635.23 3.84, 3.88 (3) 1:1 (¹H NMR) 157 Prepar- ative HPLC (Method 2) 312

Free Base 706.16 3.41, 3.45 (3) 1:1 (¹H NMR) 157 Prepar- ative HPLC (Method 2) 313

Free Base 621.2 3.63 (3) 6:4 (¹H NMR) 156 Prepar- ative HPLC (Method 2) 314

Free Base 692.28 3.23 (3) 6:4 (¹H NMR) 156 Prepar- ative HPLC (Method 2) 315

Free Base 672.13 3.42; 3.47 (3) 5:95 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.57 (s, 2 H), 7.83 (dt, 1 H), 7.72-7.79 (m, 2 H), 7.70 (td, 1 H), 7.54 (d, 1 H), 7.43 (d, 1 H), 7.26 (dd, 1 H), 6.04 (dd, 1 H), 4.19 (dd, 1 H), 3.49 (dd, 1 H), 3.32-3.44 (m, 1 H), 3.28 (dd, 1 H), 3.19 (dt, 1 H), 3.02 (br. S., 3 H), 2.90 (br. S., 3 H), 1.90-2.07 (m, 1 H), 1.46-1.81 (m, 3 H) −67.58, (c = 0.47, DCM 172 Prepar- ative HPLC (Method 2) 316

Free Base 649.35 3.97 (3) 1:1 (¹H NMR) 173 SCX cartridge followed by preparatibe HPLC (Mehtod 2) 317

Free Base 720.43 3.56 (3) 1:1 (¹H NMR) 173 SCX cartridge followed by preparatibe HPLC (Mehtod 2)

Example 35 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (320)

Step 1: (S)-ethyl 3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylate (318)

(S)-ethyl thiazolidine-2-carboxylate (2R,3R)-2,3-dihydroxysuccinate (prepared as described in Bull. Korean Chem. Soc., 2010, 31, 2709, which is incorporated herein by reference in its entirety), (4 g, 12.85 mmol) was poured into a separation funnel containing aqueous sat. NaHCO₃ (50 ml, 55.0 mmol) and Et₂O (100.0 ml), previously cooled to 0° C. in an ice bath. The mixture was shaken to dissolution of the solid; the phases were separated, and the aqueous layer was extracted again with Et₂O (100 ml). The combined organic layers were dried over Na₂SO₄ and evaporated to dryness without heating. The residue was dissolved in THF (50 ml), the solution was cooled to 0° C., and aqueous sat. NaHCO₃ (50 ml, 55.0 mmol) was added. A solution of 3-(dimethylcarbamoyl)benzene-1-sulfonyl chloride (3.18 g, 12.85 mmol) in THF (50 ml) was added to the biphasic mixture at 0° C. under vigorous stirring, and the reaction was left at RT for 4 hours. The mixture was partitioned between EtOAc and water, and the aqueous layer was extracted with EtOAc. The combined organic layers were washed with aqueous 1N HCl and brine, dried over Na₂SO₄ and evaporated to dryness to afford (S)-ethyl 3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylate (3.79 g, 10.18 mmol, 79% yield); MS/ESI⁺ 373.04 [MH]⁺

Step 2: (S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylic acid (319)

(S)-ethyl 3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylate (3.79 g, 10.18 mmol) was dissolved in mixture of MeOH (30 ml), THF (30.0 ml), and water (30.0 ml). LiOH (0.487 g, 20.35 mmol) was added, and the reaction was stirred at RT for 30 minutes. The mixture was acidified with aqueous 1N HCl (pH=1), diluted with water, and extracted twice with EtOAc. The combined organic layers were dried over Na₂SO₄ and evaporated to dryness. The residue was triturated with a mixture of Et₂O (15 ml) and petroleum ether (25 ml) yielding after filtration (S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylic acid (1.86 g, 5.40 mmol, 53.1% yield); MS/ESI⁺ 344.94 [MH]⁺; [α_(D)]=−36.1 (c=1.67, MeOH). To determine the enantiomeric purity, this intermediate was coupled with alcohol 1 (EDC, DMAP, DCM) to afford compound 52: Diastereomeric Ratio=95:5.

Step 3: 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (320)

To a solution of 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-hydroxyethyl)pyridine 1-oxide (156) (160 mg, 0.416 mmol), EDC (160 mg, 0.833 mmol), and DMAP (102 mg, 0.833 mmol) in DCM (50 ml), (S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylic acid (172 mg, 0.500 mmol) was added, and the resulting mixture was stirred at RT for 24 hours. The reaction mixture was washed twice with aqueous 1N HCl, and the organic layer was dried over Na₂SO₄. The solvent was removed under vacuum, and the residue was purified by preparative HPLC (Method 2) to afford 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide (122 mg, 0.172 mmol, 41% yield); MS/ESI⁺ 710.25 [MH]⁺, t_(R)=3.25 min (Method 3); Diastereomeric Ratio 1:1 (¹H NMR).

The compounds listed in Table 26 were prepared according to Scheme 41 using commercial suitable reagents and by reacting the appropriate alcohol listed, followed by appropriate purification step as below reported. The enantiomeric purity of intermediate obtained using benzenesulfonylchloride was determined as described above in Step 2 (reference compound: 89; Diastereomeric Ratio=92:8)

TABLE 26 HPLC-MS characterization Alco- t_(R)/min Dia- hol Method stereo- Pre- Purifi- En- SALT MS/ESI⁺ 1, 2 meric cur- cation try Structure NAME [MH]⁺ or 3 ratio ¹H NMR [α]_(D) sor Method 321

Free Base 639.08 3.66, 3.69 (3) 1:1 (¹H NMR) 156 Prepar- ative HPLC (Method 2) 322

Free Base 653.08 3.91, 3.96 (3) 1:1 (¹H NMR) 157 Prepar- ative HPLC (Method 2) 323

Free Base 724.26 3.48, 3.52 (3) 1:1 (¹H NMR) 157 Prepar- ative HPLC (Method 2) 324

Free Base 599.22 3.23 (3) >95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d6) δ ppm 8.58 (s, 2 H), 7.83-7.92 (m, 2 H), 7.72-7.81 (m, 1 H), 7.60-7.71 (m, 2 H), 6.95 (d, 1 H), 6.88 (dd, 1 H), 6.00 (dd, 1 H), 5.41 (s, 1 H), 3.78-3.86 (m, 1 H), 3.77 (s, 3 H), 3.75 (s, 3 H), 3.57- 3.71 (m, 1 H), 3.48 (dd, 1 H), 3.30 (dd, 1 H), 2.88-3.14 (m, 1 H), 2.64 (dt, 1 H) −60.50 (c = 0.4, DCM) 170 Prepar- ative HPLC (Method 2) 325

Free Base 670.17 2.83 (3) 95:5 (¹H NMR) ¹H NMR (300 MHz, DMSO-d₆) δ ppm 8.56 (s, 2 H), 7.93 (dt, 1 H), 7.90 (t, 1 H), 7.77 (dt, 1 H), 7.71 (t, 1 H), 6.95 (d, 1 H), 6.94 (d, 1 H), 6.88 (dd, 1 H), 6.00 (dd, 1 H), 5.51 (s, 1 H), 3.81- 3.96 (m, 1 H), 3.76 (s, 3 H), 3.75 (s, 3 H), 3.58-3.70 (m, 1 H), 3.48 (dd, 1 H), 3.31 (dd, 1 H), 3.02 (br. S., 3 H), 2.92-3.02 (m, 1 H), 2.89 (br. S., 3 H), 2.64 (dt, 1 H) −50.25 (c = 0.40, DCM) 170 Prepar- ative HPLC (Method 2) 326

Free Base 667.31 4.05 (3) 1:1 (¹H NMR) 174 SCX cartridge followed by preparative HPLC (Method 2) 327

Free Base 738.39 3.63 1:1 (¹H NMR) 174 SCX cartridge followed by preparative HPLC (Method 2)

Pharmacological Activity of the Compounds of the Invention Example 15 In Vitro Determination of PDE4 Inhibitory Activity in the Cell Free Assay

PDE4 activity was determined in U937 human monocytic supernatants cells lysate. Cells were cultured, harvested and supernatant fraction prepared essentially as described in Torphy T J, et al., 1 J. Pharmacol. Exp. Ther., 1992; 263:1195-1205, which is incorporated herein by reference in its entirety. U937 cells (Cell Bank, Interlab Cell Line Collection, ICLC HTL94002) were grown at 37° C., 5% CO₂ in RPMI 1640 with GlutaMAX™-I medium supplemented with 10% fetal bovine serum and 100 μg/ml Pen-strep (Gibco). Cells were harvested and washed twice by centrifugation (150×g, 8 minutes) in cold PBS. Washed cells were resuspended in cold Krebs-Ringer-Henseleit buffer at a final concentration 20×10⁻⁶ cells/ml and sonicated. After centrifugation at 15000×g for 20 min, the supernatants were pooled, divided in aliquots and stored at −80° C.

PDE4 activity was determined in cells supernatants by assaying cAMP disappearance from the incubation mixtures. The concentration of the test compounds ranged between 10⁻¹² M and 10⁻⁶ M. Reactions were stopped by enzyme heat inactivation (2.5 minutes at 100° C.), and residual cAMP content was determined using the ‘LANCE cAMP Assay’ from PerkinElmer following the providers instructions. The results of the tested compounds, representatives of the invention, expressed as mean±standard deviation of the nM concentration of the test compound producing 50% inhibition of cAMP disappearance (IC₅₀) are shown in the following Table:

PDE4 Compound No. inhibition 209, 234, 238, 239, 240, 241, 242, 227, 228, 206, 207, ++++ 269, 198, 271, 295, 210, 186, 244, 185, 281, 232, 218, 219, 220, 309, 310, 287, 288, 305, 283, 250, 314, 301, 302, 224, 300, 287, 288, 226, 299, 312, 285, 308, 189, 264, 278, 225, 191, 256, 274, 266, 275, 291, 195, 190, 237, 15, 17, 30, 31, 32, 33, 34, 38, 42, 52, 53, 54, 55, 56, 58, 64, 65, 66, 73, 75, 77, 78, 82, 84, 85, 88, 90, 91, 93, 94, 97, 100, 101, 102, 106, 107, 109, 110, 114, 118, 119, 121, 123, 124, 125, 126, 127, 128, 129, 130, 131, 132, 135, 137, 138, 139, 141, 143, 150, 151 200, 201, 202, 203, 204, 205, 208, 229, 263, 284, 307, +++ 311, 257, 292, 258, 199, 281, 19, 49, 57, 59, 62, 63, 67, 68, 69, 70, 71, 72, 74, 76, 79, 80, 81, 83, 86, 89, 103, 104, 105, 108, 136, 144 245, 246, 248, 249, 315, 303, 26 ++

In the table above, PDE4 binding potencies (IC₅₀ values) are indicated as follows: >10 nM “+”; 10-1 nM “++”; 1-0.1 nM “+++”; <0.1 nM “++++”.

Percentage of inhibition of PDE4 activity was calculated, assuming cAMP disappearance in the absence of inhibitors as 100% and cAMP disappearance in heat inactivated samples as 0%.

Analogously, results for tested compounds of formula (II) (expressed as mean±standard deviation of the nM concentration of the test compound producing 50% inhibition of cAMP disappearance) (IC₅₀) are shown in the following Table:

Compound No. PDE4 inhibition 8, 11, +++ 3, 9, 10, 14 ++

In the table above, PDE4 binding potencies (IC₅₀ values) are indicated as follows: >10 nM “+”; 10-1 nM “++”; 1-0.1 nM “+++”; <0.1 nM “++++”.

Example 16 In Vitro Determination of PDE4 Inhibitory Activity in the Peripheral Blood Mononuclear Cells (PBMCs) Assay

The assay, which is based on the known inhibitory activity exerted by PDE4 inhibitors on the lipopolyshaccarides (LPS)-induced tumour necrosis factor-alpha (TNF-α release in peripheral blood mononuclear cells (PBMCs), was performed according to a method previously described (Hatzelmann A et al., J. Pharmacol. Exp. Ther., 2001; 297:267-279; and Draheim R et al., J. Pharmacol. Exp. Ther., 2004; 308:555-563, which are incorporated herein by reference in their entireties). Cryopreserved human PBMCs, (100 μl/well) were incubated in 96-well plates (10⁵ cells/well), for 30 minutes, in the presence or absence (50 microl) of the test compounds whose concentrations ranged from 10⁻¹² M to 10⁻⁶ M or from 10⁻¹³ M to 10⁻⁷ M. Subsequently, LPS (3 ng/ml) was added.

After 18 hours of incubation at 37° C. in a humidified incubator under an atmosphere of 95% air and 5% CO₂, culture medium was collected and TNF-α measured by ELISA. The results of the tested compounds, representatives of the invention, expressed as mean±95% confidence limits of the molar concentration of the test compound producing 50% inhibition of LPS-induced TNF-α release (IC₅₀) are shown in the following Table:

PDE4 Compound No. inhibition 239, 240, 241, 242, 206, 271, 210, 310, 250, 251, 252, ++++ 269, 287, 299, 35, 37, 38, 52, 54, 56, 59, 64, 66, 73, 74, 82, 83, 84, 85, 88, 90, 91, 92, 93, 94, 95, 96, 97, 101, 106, 107, 109, 113, 115, 116, 118, 119, 123, 124, 128, 129, 130, 131, 132, 133, 139, 140, 150, 155 238, 201, 203, 228, 207, 198, 209, 295, 243, 186, 187, +++ 185, 281, 253, 288, 200, 16, 17, 20, 22, 26, 31, 32, 34, 36, 39, 40, 41, 49, 51, 53, 55, 57, 58, 60, 61, 62, 63, 65, 67, 68, 69, 70, 75, 76, 77, 78, 79, 80, 81, 86, 87, 89, 98, 103, 104, 105, 108, 110, 111, 114, 117, 121, 125, 126, 127, 135, 136, 137, 138, 141, 142, 143, 144, 151 244, 263, 15, 19, 21, 30, 71, 99, 100 ++

In the table above, PDE4 binding potencies (IC₅₀ values) are indicated as follows: >10 nM “+”; 10-1 nM “++”; 1-0.1 nM “+++”; <0.1 nM “++++”.

The effects of the tested compounds were calculated as percentage of inhibition of TNF-α release, assuming LPS-induced TNF-α production in the absence of inhibitor compound as 100% and basal TNF-α production of PBMCs in the absence of LPS as 0%.

Analogously, results of tested compounds for compounds of formula (II) expressed as mean±95% confidence limits of the molar concentration of the test compound producing 50% inhibition of LPS-induced TNF-α release (IC₅₀) are shown in the following Table:

Compound No. PDE4 inhibition 6, 11 +++ 8, 9, ++

In the table above, PDE4 binding potencies (IC₅₀ values) are indicated as follows: >10 nM “+”; 10-1 nM “++”; 1-0.1 nM “+++”; <0.1 nM “++++”.

Where a numerical limit or range is stated herein, the endpoints are included. Also, all values and subranges within a numerical limit or range are specifically included as if explicitly written out.

Obviously, numerous modifications and variations of the present invention are possible in light of the above teachings. It is therefore to be understood that, within the scope of the appended claims, the invention may be practiced otherwise than as specifically described herein.

All patents and other references mentioned above are incorporated in full herein by this reference, the same as if set forth at length. 

1. A compound of formula (I):

wherein: R₁ is: H; (C₃-C₇)cycloalkylcarbonyl; (C₁-C₆)alkyl, optionally substituted by one or more substituents selected from (C₃-C₇) cycloalkyl or (C₅-C₇)cycloalkenyl; (C₁-C₆)haloalkyl; (C₃-C₇)cycloalkyl; (C₅-C₇)cycloalkenyl; (C₂-C₆)alkenyl; or (C₂-C₆)alkynyl; R₂ is: H; (C₃-C₇)cycloalkylcarbonyl; (C₁-C₆)alkyl, optionally substituted by one or more substituents selected from (C₃-C₇) cycloalkyl or (C₅-C₇)cycloalkenyl; (C₁-C₆)haloalkyl; (C₃-C₇)cycloalkyl; (C₅-C₇)cycloalkenyl; (C₂-C₆)alkenyl; or (C₂-C₆)alkynyl; or, when R₁₉ is different from hydrogen, R₂ forms together with R₁₉ a group of formula (x) as defined below; or R₁ and R₂, together with the interconnecting atoms, form a 2,2-difluoro-1,3-dioxolane ring of formula (q) fused to the phenyl moiety which bears groups —OR₁ and —OR₂, wherein asterisks indicate carbon atoms shared with such phenyl ring:

R₁₉ is hydrogen or, if different from hydrogen, it forms together with R₂ a group of formula (x) wherein bonds labeled with (1) and (2) indicate the points of attachment for group (x) to atoms bearing groups R₁₉ and R₂ respectively

in such a way that R₂ and R₁₉ together with the interconnecting atoms form a ring of formula (w) which is fused to phenyl ring which bears groups —OR₂ and R₁₉, wherein asterisks indicate carbon atoms shared with such phenyl ring:

R₃ is one or more substituents independently selected from the group consisting of H, CN, NO₂, CF₃ and a halogen atom; Z is a group —(CH₂)_(n)— wherein n is 0 or 1; A is a saturated and monocyclic (C₃-C₇)heterocycloalkyl-ene group; K is: —(CH₂)_(m)C(O)R₄ wherein m may be 0 or 1; —C(O)(CH₂)_(j)R₄, wherein j may be 1 or 2; —SO₂ (CH₂)_(p)R₄ wherein p may be zero, 1 or 2; —(CH₂)_(y)SO₂R₄ wherein y may be 1 or 2; —(CH₂)_(n)R₄ wherein z may be 1 or 2; or —C(O)(CH₂)₂SO₂R₄; R₄ is a ring system, that is a mono- or bicyclic ring which may be saturated, partially unsaturated or fully unsaturated, such as aryl, (C₃-C₈)cycloalkyl, (C₃-C₇) heterocycloalkyl, or heteroaryl, such ring being optionally substituted by one or more groups R₅ which may be the same or different, and which are independently selected from the group consisting of: (C₁-C₆)alkyl optionally substituted by one or more groups independently selected in the list consisting of: (C₃-C₇)cycloalkyl, —OH and a group —NR₁₈C(O)(C₁-C₄)alkyl, wherein R₁₈ is hydrogen or (C₁-C₄)alkyl; (C₃-C₇)heterocycloalkyl; 5 or 6-membered heteroaryl which is optionally substituted by one or two (C₁-C₄)alkyl groups; (C₁-C₆)haloalkyl; (C₃-C₇)heterocycloalkyl(C₁-C₄)alkyl; a group —OR₆ wherein R₆ is H; (C₁-C₆)haloalkyl; a group —SO₂R₇, wherein R₇ is (C₁-C₄)alkyl; a group —C(O)R₇ wherein R₇ is (C₁-C₄)alkyl; (C₁-C₁₀)alkyl optionally substituted by one or more (C₃-C₇) cycloalkyl groups or by a group —NR₈R₉ as below defined; or (C₃-C₇)cycloalkyl; a group —SR₂₀ wherein R₂₀ is H; (C₁-C₆)haloalkyl; a group —C(O)R_(D) wherein R₇ is (C₁-C₄)alkyl; (C₁-C₁₀)alkyl optionally substituted by one or more (C₃-C₇) cycloalkyl groups or by a group —NR₈R₉; or (C₃-C₇)cycloalkyl; a halogen atom; CN; NO₂; NR₈R₉ wherein R₈ and R₉ are different or the same and are independently selected from the group consisting of: H; (C₁-C₄)alkylene-NR₁₃R₁₄ wherein R₁₃ and R₁₄ are different or the same and are independently selected from the group consisting of: H and (C₁-C₆)alkyl, which is optionally substituted with (C₃-C₇) cycloalkyl or (C₃-C₇)heterocycloalkyl; or they form with the nitrogen atom to which they are linked a saturated or partially saturated (C₃-C₇)heterocyclic ring; (C₁-C₆)alkyl, optionally substituted with (C₃-C₇)cycloalkyl, (C₃-C₇)heterocycloalkyl, a group —OH or (C₁-C₆)alkoxyl; a group —SO₂R₁₅, wherein R₁₅ is selected in the group consisting of: (C₁-C₄)alkyl optionally substituted by (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl; (C₃-C₇)heterocycloalkyl; and phenyl optionally substituted by one or more (C₁-C₆)alkyl, halogen or a group —OH; a group —C(O)R₁₆, wherein R₁₆ is selected in the group consisting of: (C₁-C₆)alkyl optionally substituted by (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl; (C₃-C₇)heterocycloalkyl; phenyl optionally substituted by one or more (C₁-C₆)alkyl, halogen or —OH; and a group —NH₂; a group —C(O)OR₁₇, wherein R₁₇ is selected in the group consisting of: (C₁-C₆)alkyl optionally substituted by (C₃-C₇)cycloalkyl or (C₃-C₇)heterocycloalkyl; (C₃-C₇)heterocycloalkyl; phenyl optionally substituted by one or more (C₁-C₆)alkyl, halogen or —OH; and a group —NH₂; or they form with the nitrogen atom to which they are linked a saturated or partially saturated heterocyclic ring, which is optionally substituted by one or more (C₁-C₆)alkyl or oxo groups; (C₁-C₄)alkylene-NR₈R₉ as above defined; COR₁₀ wherein R₁₀ is phenyl or (C₁-C₆)alkyl; oxo; —SO₂R₁₁ wherein R₁₁ is (C₁-C₄)alkyl, —OH or —NR₈R₉ wherein R₈ and R₉ are as defined above; —COOR₁₂ wherein R₁₂ is H, (C₁-C₄)alkyl or (C₁-C₄)alkylene-NR₈R₉ wherein R₈ and R₉ are as defined above; and —CONR₈R₉ wherein R₈ and R₉ are as defined above; wherein groups R₆, R₇, R₈, R₉, R₁₀, R₁₁, R₁₂, R₁₃, R₁₄, R₁₅, R₁₆, R₁₇, R₁₈, R₁₉, and R₂₀ may be the same or different at each occurrence, if present in more than one group; an N-oxide derivative on the pyridine ring, or a pharmaceutically acceptable salt thereof.
 2. A compound according to claim 1, which is represented by formula (IC):

an N-oxide derivative on the pyridine ring, or a pharmaceutically acceptable salt thereof.
 3. A compound according to claim 1, which is represented by formula (IF):

Wherein: Z is a bond, A is a (C₃-C₇)heterocycloalkyl-ene group comprising a nitrogen atom which represents the connecting point to group K, K is a group selected from the group consisting of:

R₄ is a phenyl group or a 5 or 6-membered heteroaryl group, each R₄ being optionally substituted by one or more groups R₅; An N-oxide derivative on the pyridine ring, or a pharmaceutically acceptable salt thereof.
 4. A pyridine N-oxide according to claim 1, which is represented by formula (IH):

or a pharmaceutically acceptable salt thereof.
 5. A compound according to claim 1, which is represented by formula (I)′:

an N-oxide derivative on the pyridine ring, or a pharmaceutically acceptable salt thereof.
 6. A pyridine N-oxide according to claim 1, which is represented by formula (IDa):

or a pharmaceutically acceptable salt thereof.
 7. A compound according to claim 1, which is selected from the group consisting of: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(cyclopropylmethoxy)-4-(methylsulfonamido)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(4-methoxy-3-(methylsulfonyloxy)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3,4-dimethoxyphenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(methylsulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(N-(2-morpholinoethyl)methylsulfonamido)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((R)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((S)-2-((S)-3-(4-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((S)-2-((S)-1-(4-aminophenylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-((4-(methoxycarbonyl)-5-methylfuran-2-yl)methyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R or S)-4-(3-sulfamoylphenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(2-oxo-2-(thiophen-2-yl)ethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S or R)-3-(4-(dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S or R)-3-(4-(dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(3-(4-aminobenzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(4-(3-(dimethylcarbamoyl)phenylsulfonyl)thiomorpholine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(4-(4-(N-methylsulfamoyl)phenylsulfonyl)thiomorpholine-3-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(3-(3-amino-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((R)-3-(4-aminophenylsulfonyl)thiazolidine-4-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((2S)-2-(4-(4-aminophenylsulfonyl)morpholine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(4-(3-(dimethylcarbamoyl)phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(1,3-dioxoisoindolin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-sulfamoylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(3-(3-carboxy-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-fluorophenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(2,4-dimethylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(thiophen-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(dimethylcarbamoyl)-4-methoxyphenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(4-(3-(dimethylcarbamoyl)phenylsulfonyl)piperazin-1-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(4-methylpiperazine-1-carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(3-chlorophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(1-methyl-1H-imidazol-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(cyclopropylmethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(pyridin-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(2,4-difluorophenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(2-chloro-4-fluorophenyl sulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-fluoro-2-methylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(2-chlorophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclohexyl sulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(2,4-dioxo-1,2,3,4-tetrahydroquinazolin-6-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(thiophen-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(cyclopropylmethoxy)-5-(N-(2-morpholinoethyl)methylsulfonamido)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3,4-dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-4-(2-(2-(4-(4-aminophenylsulfonyl)piperazin-1-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(6-morpholinopyridin-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-methoxy-3-(4-methylpiperazine-1-carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-methoxy-3-(morpholine-4-carbonyl)phenyl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S or R)-3-(4-methoxy-3-(morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(N,N-dimethyl sulfamoyl)-4-methoxybenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S or R)-3-(3-carboxyphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(4-(phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3,5-dimethylisoxazol-4-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(thiazole-5-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-((dimethylamino)methyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(oxazole-5-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(4-methylpiperazine-1-carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-(methoxycarbonyl)thiophen-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(pyridin-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)-4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-1H-imidazol-2-yl sulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-sulfamoylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(4-(methylsulfonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3,4-dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(5-((dimethylamino)methyl)thiophene-2-carbonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(3-(4-(2-aminoethyl)benzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(N-methylsulfamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(furan-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(furan-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(N,N-dimethylsulfamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3,4-dimethoxyphenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(pyridin-3-ylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(methoxycarbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-(methoxycarbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(trifluoromethoxy)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(1,1-dioxothiomorpholinobenzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(4-carbamoylbenzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(6-morpholinopyridin-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S or R)-3-(4-(aminomethyl)picolinoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-methoxy-4-methylphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2,4-dimethylthiazol-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-picolinoylthiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S or R)-3-(3-((2-morpholinoethoxy)carbonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(6-morpholinopyridin-3-ylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(4-nitrophenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(N,N-dimethylsulfamoyl)phenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2,5-dimethoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-1H-imidazol-2-ylsulfonyl)piperidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(3-acetylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(morpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide: 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(1,1-dioxo thiomorpholinomethyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(3-(aminomethyl)benzoyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(oxazol-5-yl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(3-aminophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(methylsulfonyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(4-methylpiperazine-1-carbonyephenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3-(3-(N-methylsulfamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-1H-imidazol-4-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-phenylacetyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(2-cyclopropylacetyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(phenylsulfonyl)propanoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-morpholinopropanoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(4-methylpiperazin-1-yl)propanoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-(2-((S)-1-benzoylpyrrolidin-2-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-((S)-1-(3-(dimethylcarbamoyl)benzoyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)acetyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-(3-(dimethylcarbamoyl)phenyl)acetyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(2-cyanophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2,3-dihydrobenzo[b][1,4]dioxin-6-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(2-cyano-5-methylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2,5-dimethylthiophen-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(4-bromo-2-fluoro-5-methylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((S)-2-((S)-3-(3-bromo-4-methylphenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(4-cyanophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(3-cyanophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(4-(1H-pyrazol-1-yl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(3-cyano-4-fluorophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-2-oxoindolin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(2-chloro-5-cyanophenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(5-methylbenzo[b]thiophen-2-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(1-methyl-1H-pyrazol-3-yl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(difluoromethoxy)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-((S)-3-(4-chloro-2-(trifluoromethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(5-fluoro-2-methoxyphenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(benzo[b]thiophen-2-ylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-oxo-2,3-dihydrobenzo[d]oxazol-6-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(2-oxopyrrolidin-1-yl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-(1-acetyl-1,2,3,4-tetrahydroquinolin-6-ylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((S)-2-((S)-3-(4-(2-acetamidoethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(4-(2,2,2-trifluoroethoxy)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-(2-((S)-3-(benzylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(phenethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-1-(benzylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(1-methyl-2-oxoindolin-5-ylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(phenylsulfonyl)piperidine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(R)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)piperidine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)piperidine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)piperidine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(R)-4-(phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(R)-4-(3-(dimethylcarbamoyl)phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-4-(phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-4-(3-(dimethylcarbamoyl)phenylsulfonyl)morpholine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-((S)-1-(phenylsulfonyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 4-((S)-2-(2-((S)-1-(benzylsulfonyl)pyrrolidin-2-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-oxo-2-phenylethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-oxo-2-phenylethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-1-benzylpyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)benzyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-(3-(dimethylcarbamoyl)phenyl)-2-oxoethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-(3-(dimethylcarbamoyl)phenyl)-2-oxoethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(cyclopropylmethyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((S)-3-benzylthiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-phenethylthiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-((S)-1-(3-(dimethylcarbamoyl)benzyl)pyrrolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-ureidophenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(hydroxymethyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((2S)-2-(2-(3-benzoylthiazolidin-2-yl)acetoxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(3-(dimethylcarbamoyl)benzoyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(phenylsulfonyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((2S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(2-(3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidin-2-yl)acetoxy)ethyl)pyridine 1-oxide; (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-3-carbonyloxy)ethyl)pyridine 1-oxide; (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(1-(phenylsulfonyl)azetidine-3-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)azetidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)azetidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(1-methyl-2-oxoindolin-5-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-morpholinoethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(2-(4-methylpiperazin-1-yl)ethylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-(phenylsulfonyl)ethyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(2-phenylacetyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S or R)-2-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-methoxyphenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopentyloxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-(1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-(1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S or R)-2-(2,2-difluorobenzo[d][1,3]dioxol-5-yl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-'7-yl)-2-((S)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)-2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopropylmethoxy)-4-methoxyphenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(3-(cyclopentyloxy)-4-methoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3,4-dimethoxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-'7-yl)-2-((S)-3-(phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-(2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)-2-(4-methoxyspiro[benzo[d][1,3]dioxole-2,1′-cyclopentane]-7-yl)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(N,N-dimethylsulfamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-methylisoxazolo[5,4-b]pyridin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1,3-dimethyl-1H-pyrazolo[3,4-b]pyridin-5-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(1-methyl-5-(methylcarbamoyl)-1H-pyrrol-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(5-(pyrrolidine-1-carbonyl)-1H-pyrrol-3-ylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-((S)-1-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3,5-dichloropyridin-4-yl)ethyl) 3-(1-methyl-1H-imidazol-2-ylsulfonyl)thiazolidine-2-carboxylate; 4-((S)-2-((S)-3-(1H-1,2,4-triazol-5-ylsulfonyl)thiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 4-((S)-2-((S)-3-benzoylthiazolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)benzoyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 4-((S)-2-((R)-1-benzoylpyrrolidine-2-carbonyloxy)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)ethyl)-3,5-dichloropyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(3-(dimethylcarbamoyl)benzoyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-(dimethylcarbamoyl)phenylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; (S)-((S)-1-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-(3,5-dichloropyridin-4-yl)ethyl) 3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carboxylate; 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((R)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(4-(difluoromethoxy)-3-hydroxyphenyl)-2-((S)-3-(3-(dimethylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-1-(3-methylisoxazolo[5,4-b]pyridin-5-ylsulfonyl)pyrrolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(4-methyl-3,4-dihydro-2H-benzo[b][1,4]oxazin-6-ylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide; 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((R)-3-(3-methylisoxazolo[5,4-b]pyridin-5-ylsulfonyl)thiazolidine-4-carbonyloxy)ethyl)pyridine 1-oxide; and 3,5-dichloro-4-((S)-2-(3-(cyclopropylmethoxy)-4-(difluoromethoxy)phenyl)-2-((S)-3-(3-(methylcarbamoyl)phenylsulfonyl)thiazolidine-2-carbonyloxy)ethyl)pyridine 1-oxide; or a pharmaceutically acceptable salt thereof.
 8. A process for preparing a compound of formula (IDa) according to claim 6, comprising: (1) reacting a compound of formula (XV) with a compound of formula (XIV), to obtain a compound of formula (XII):

by: a) adding a compound of formula (XIV), 4-dimethylaminopyridine, and 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide) hydrochloride to a solution of a compound of formula (XV) in dimethylformamide, to obtain a mixture; b) stirring said mixture; c) pouring the mixture into cold water, to obtain a precipitate; and d) filtering the precipitate; (2) converting said compound of formula (XII) to a compound of formula (XI):

by: a) adding, with stirring, a solution of concentrated HCl in dry ethyl acetate (9 vol.) to a solution of said compound of formula (XII) in ethyl acetate at room temperature; b) stirring, to obtain a precipitated solid; c) filtering said precipitated solid; and optionally d) washing said precipitated solid with ethyl acetate; and (3) reacting said compound of formula (XI) with a compound of formula (VII), to obtain said compound of formula (IDa):

by: a) adding a solution of a compound of formula (VII) in pyridine to a refrigerated solution of said compound of formula (XI), in pyridine; b) stirring the resulting solution at room temperature; c) pouring the solution into aqueous HCl in excess, to obtain a precipitate; d) filtering said precipitated material and washing it with water or d′) extracting the aqueous phase with ethyl acetate, washing with HCl 1M, brine and evaporating the resulting organic phase; f) dissolving the compounds in ethanol (8 vol); g) vigorously stirring overnight at room temperature; and h) filtering the solid formed; wherein R₁, R₂, R₃, R₄ and p in compounds of formulas (XV), (XIV), (XII), (XI), (VII) and (IDa) have meanings as per compounds of formula (I).
 9. A combination of a compound, N-oxide, or pharmaceutically acceptable salt according to claim 1 with a second pharmaceutical active component selected from the group consisting of a beta2-agonist, a corticosteroid, and an antimuscarinic agent.
 10. A pharmaceutical composition, comprising a compound, N-oxide, or pharmaceutically acceptable salt according to claim 1 and one or more pharmaceutically acceptable carriers and/or excipients.
 11. A pharmaceutical composition, comprising a combination according to claim 9 and one or more pharmaceutically acceptable carriers and/or excipients.
 12. A method for prevention and/or treatment of a disease of the respiratory tract characterized by airway obstruction, such as asthma or COPD, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, N-oxide, or pharmaceutically acceptable salt according to claim
 1. 13. A method for prevention and/or treatment of allergic rhinitis, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, N-oxide, or pharmaceutically acceptable salt according to claim
 1. 14. A method for prevention and/or treatment of atopic dermatisis, said method comprising administering to a patient in need of such treatment a therapeutically effective amount of a compound, N-oxide, or pharmaceutically acceptable salt according to claim
 1. 15. A device comprising a pharmaceutical composition according to claim
 10. 16. A device comprising a pharmaceutical composition according to claim
 11. 17. A kit comprising a pharmaceutical composition according to claim 10 and a device which is a single- or multi-dose dry powder inhaler, a metered dose inhaler, or a soft mist nebulizer.
 18. A kit comprising a pharmaceutical composition according to claim 11 and a device which is a single- or multi-dose dry powder inhaler, a metered dose inhaler, or a soft mist nebulizer. 